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1.
Recenti Prog Med ; 87(4): 145-9, 1996 Apr.
Article in Italian | MEDLINE | ID: mdl-8643873

ABSTRACT

The question whether influenza vaccine could lead to a clinical flare in patients with rheumatoid arthritis (RA), and whether it could induce an effectively protective antibody response to the infection is still much debated. Based on these data, we have performed an open study in 40 patients with RA. Patients were divided into two groups according to their disease activity (those with RA in remission and those with active RA, respectively), and their clinical and serum antibody response was assessed following the vaccine administration in the 1991-92 winter seasons. A group of age and sex matched, healthy controls were also vaccinated. Our results suggest that immunization against influenza does not modify the clinical picture of RA, even though some differences between the two groups mentioned above were noticed. In addition, side-effects or adverse reactions occurred with similar frequency in patients with RA and in the controls; as to the antibody response in patients with RA, in the majority of cases the immune response proved adequate to provide significant protection from the infection.


Subject(s)
Arthritis, Rheumatoid/immunology , Influenza Vaccines/administration & dosage , Influenza, Human/immunology , Vaccination , Aged , Antibody Formation , Female , Humans , Immunization Schedule , Influenza Vaccines/adverse effects , Influenza Vaccines/immunology , Influenza, Human/prevention & control , Italy , Male , Middle Aged
2.
Minerva Med ; 86(11): 467-4, 1995 Nov.
Article in Italian | MEDLINE | ID: mdl-8684670

ABSTRACT

A group of 104 workers were examined. They were employed in selecting rags and separating the lining from wollen fabrics to be used again as thread waste in the textile industry. The aim of the study was to point out tendon and joint related disorders of the upper limb due to repetitive and forced movements. Twenty-eight (26.9%) workers complained of hand and wrist echography and thermography. In 19 patients (67.8%) clinical carpal tunnel syndrome was diagnosed. Eight workers (28.5%) had Dupuytren's contracture. Swelling of the fingers was found in 23 (82.1%). 14.2% and 28.5% of the workers showed respectively acro-osteolysis and acrosclerosis. The textile industry of Prato shows peculiar characters: the workers employed in selecting rags out a manual job which causes soft tissues and skeletal disorders in a great number of them. The acro-osteolytic and acrosclerotic changes of the fingers seem alike the bone disorders of chronic inflammatory rheumatic diseases as seronegative spondyloarthritis.


Subject(s)
Cumulative Trauma Disorders/etiology , Finger Injuries/etiology , Hand Injuries/etiology , Occupational Diseases/etiology , Textile Industry , Wrist Injuries/etiology , Carpal Tunnel Syndrome/diagnosis , Carpal Tunnel Syndrome/etiology , Dupuytren Contracture/diagnosis , Dupuytren Contracture/etiology , Female , Hand Injuries/diagnosis , Humans , Italy , Male , Middle Aged , Osteoarthritis/diagnosis , Osteoarthritis/etiology , Syndrome , Textiles , Wrist Injuries/diagnosis
3.
Clin Exp Rheumatol ; 12(2): 163-8, 1994.
Article in English | MEDLINE | ID: mdl-8039283

ABSTRACT

OBJECTIVE: Treatment of SLE exacerbations with intravenous gammaglobulins has been shown to be safe and effective, leading to both clinical and serological improvement. In this study we test the hypothesis that intravenous immunoglobulins (IVIg), administered over a long period, would also be effective in patients with chronically active SLE. DESIGN AND PATIENTS: An open trial was carried out on 12 patients with SLE refractory to conventional treatments, administering monthly infusions of intravenous immunoglobulins at a dose of 400 mg/kg/day for 5 consecutive days. The therapy (400 mg/kg for 5 days) lasted from 6 up to 24 months. RESULTS: Progressive clinical improvement was observed in 11 patients during the entire treatment course. This improvement was associated with an increase in hemoglobin, total serum hemolytic complement activity and C3 and C4 components, and in 2 thrombocytopenic patients in the platelet count, as well as a progressive reduction of ESR, serum immunocomplexes and antinuclear antibodies. A marked improvement in serum urea, creatinine clearance and proteinuria was also observed in those patients with renal involvement. We did not observe any adverse effects. CONCLUSION: The results obtained suggest that IVIg therapy may be a promising option in the treatment of chronically active SLE; however, further evaluation of this therapy is essential.


Subject(s)
Immunoglobulins, Intravenous , Lupus Erythematosus, Systemic/therapy , Adolescent , Adult , Antigen-Antibody Complex/analysis , Female , Humans , Immunoglobulins/analysis , Immunoglobulins, Intravenous/adverse effects , Lupus Erythematosus, Systemic/blood , Lupus Erythematosus, Systemic/physiopathology , Male , Methylprednisolone/administration & dosage , Methylprednisolone/therapeutic use , Middle Aged , Time Factors , Treatment Outcome
4.
Recenti Prog Med ; 84(10): 679-86, 1993 Oct.
Article in Italian | MEDLINE | ID: mdl-8235034

ABSTRACT

BACKGROUND: Treatment of several autoimmune diseases with intravenous gammaglobulins (IvIg) has been demonstrated to be safe and effective in determining clinical improvement and decreasing autoantibody titer. We tested the hypothesis that IvIg would be effective in patients with Systemic Lupus Erythematosus (SLE). METHODS: We conducted an open trial involving 12 patients with SLE refractory to conventional treatments with monthly infusion of IvIg at a dosage of 400 mg/kg/day for 5 consecutive days. The duration of the therapy with the same dose every 4 weeks was from 16 to 24 months. RESULTS: A progressive clinical improvement was observed in 11 patients during IvIg therapy, and it persisted during the all period of treatment. The clinical improvement was associated with an increase of haemoglobin, albumin levels, total serum complement and C3 and C4 components, platelets count in 2 thrombocytopenic patients, and a progressive reduction of ESR, plasma immunocomplexes and antinuclear antibodies. A marked improvement in serum urea, creatinine clearance and proteinuria was also observed in the patients with renal involvement. We have not observed any adverse effects with the long-term use of this treatment. Several mechanisms have been postulated to explain the effect of IVIg in the treatment of autoimmune diseases. Many experimental and clinical data support the interesting hypothesis that IVIg may be effective in some autoimmune diseases by restoring a normal function or the physiological immune network through the same regulatory mechanisms leading to a suppression of autoimmune disorders in normal individuals. The presence of a wide spectrum of anti-idiotypic antibodies in IVIg could regulate T and B-cell activities preventing the emergence of B-cell clones with specificity for autoantigens epitopes and down-regulating autoantibodies production. CONCLUSION: The results obtained suggest that IvIg therapy seems to be a promising and beneficial approach in the treatment of SLE. However, double-blind studies are necessary to confirm the results obtained particularly to ascertain the optimal dosage, the schedule of infusion and the duration of maintenance therapy with IVIg, and to determine their long-term effectiveness, the reduction in late morbidity and mortality and the effect on the quality of life of patients with SLE. Moreover, because of the high cost of IVIg, their use seems to be especially indicated for patients non responders to conventional treatments and for these with infectious complications.


Subject(s)
Immunoglobulins, Intravenous/therapeutic use , Lupus Erythematosus, Systemic/therapy , Acute Disease , Adolescent , Adult , Chi-Square Distribution , Chronic Disease , Drug Evaluation , Female , Humans , Lupus Erythematosus, Systemic/blood , Lupus Erythematosus, Systemic/epidemiology , Lupus Erythematosus, Systemic/immunology , Male , Middle Aged , Remission Induction , Time Factors
5.
Clin Ter ; 142(2): 135-40, 1993 Feb.
Article in Italian | MEDLINE | ID: mdl-8472527

ABSTRACT

To help fibromyalgia syndrome's diagnosis, the authors propose the use of Back Pain Classification Scale (BPCS), verbal test for pain analysis, able to distinguish between organic and functional disease. Two-hundred patients suspected for fibromyalgia and forty controls completed the questionnaire and so it was possible correctly to distinguish patients with organic disease from those affected by fibromyalgia. The authors conclude that BPCS can represent a useful tool for fibromyalgia diagnosis.


Subject(s)
Back Pain/classification , Fibromyalgia/diagnosis , Adult , Back Pain/diagnosis , Back Pain/etiology , Evaluation Studies as Topic , Female , Fibromyalgia/complications , Humans , Male , Middle Aged , Pain Measurement
6.
Clin Ter ; 131(5): 315-9, 1989 Dec 15.
Article in Italian | MEDLINE | ID: mdl-2532585

ABSTRACT

The antalgic activity of a newly characterized NSAID (cinnoxicam) was evaluated by cutaneous sensimetry. A precocious and significant increase in pain threshold was demonstrated by the algometric data observed after oral administration of one tablet of the drug under examination in both healthy volunteers and in rheumatic patients.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Pain Measurement/drug effects , Piroxicam/analogs & derivatives , Administration, Oral , Adult , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Drug Evaluation , Female , Humans , Male , Middle Aged , Piroxicam/administration & dosage , Piroxicam/pharmacology , Rheumatic Diseases/drug therapy , Rheumatic Diseases/physiopathology
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