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1.
Eur J Intern Med ; 16(8): 612-4, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16314250

ABSTRACT

Allergic reactions to corticosteroids are unexpected as they seem to contradict their pharmacodynamic action. Nevertheless, they are not infrequent, with an estimated incidence of up to 4% for cutaneous reactions. Systemic reactions are rarely reported, but their incidence might be underestimated. We report here an unusual allergic reaction to betamethasone presenting with diffuse bone pain, erythema, and bronchoconstriction, which was confirmed by a positive rechallenge in a double-blind procedure. This is the first case report of a systemic reaction to betamethasone confirmed by a positive rechallenge. An impurity in betamethasone diproprionate cannot be excluded. As this substance is frequently used in rheumatologic soft-tissue injections, it is important to recognize this potentially life-threatening side effect.

2.
J Investig Allergol Clin Immunol ; 11(3): 149-56, 2001.
Article in English | MEDLINE | ID: mdl-11831445

ABSTRACT

Specific immunotherapy (SIT) with standardized allergenic extracts is the only specific treatment of allergic patients. In order to evaluate the safety, side effects, and efficacy of SIT with standardized extracts adsorbed to aluminium hydroxide manufactured by Stallergènes S.A., a prospective multicenter open study was performed in Switzerland. Fifteen patients suffering from seasonal or perennial rhinoconjunctivitis with or without asthma were included in the trial and received a total of 442 injections with standardized mix of grass pollens (n = 8) or house dust mites (n = 7) over one year. Low incidence of local reactions was noted (7%). Subcutaneous nodules (granuloma) following injections were not recorded. Only a few systemic reactions (one mild rhinitis, one mild asthma attack, one worsening of eczema) were recorded. No anaphylactic reactions requiring adrenaline were recorded. No admission to the hospital was required. Global appreciation of the physicians and the patients after the first year of treatment showed a good efficacy of SIT: Only two patients (13%) did not improve. A worsening of the symptoms was not observed. In order to assess the efficacy, skin reactivity and conjunctival reactivity to allergen challenge were compared before and after one year of treatment as well as immunologic parameters (such as specific IgE, specific IgG4) in blood samples. A significant decrease in skin reactivity (p = .001) and in conjunctival reactivity (p = .01) was observed. Specific IgE level decreased for both types of allergens but to a significantly greater extent for grass pollen allergen (p = .03). Specific IgG4 level increased significantly for grass (p = 0.01) and for mites (p = 0.04). Specific immunotherapy appears to be a valuable tool in the efficient management of the allergic respiratory diseases.


Subject(s)
Allergens/therapeutic use , Desensitization, Immunologic/methods , Rhinitis, Allergic, Perennial/therapy , Rhinitis, Allergic, Seasonal/therapy , Adult , Allergens/isolation & purification , Asthma/immunology , Asthma/therapy , Desensitization, Immunologic/adverse effects , Desensitization, Immunologic/standards , Female , Humans , Immunoglobulin E/blood , Immunoglobulin G/blood , Male , Middle Aged , Prospective Studies , Rhinitis, Allergic, Perennial/immunology , Rhinitis, Allergic, Seasonal/immunology , Safety , Skin Tests
4.
Arthritis Care Res ; 11(2): 116-23, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9668734

ABSTRACT

OBJECTIVE: To compare the validity of self-reported questionnaires as response criteria of treatment efficacy in patients with fibromyalgia syndrome. METHOD: At the beginning of the treatment period, 70 fibromyalgia patients, randomly allocated to electro-acupuncture or placebo, underwent a clinical evaluation by rheumatologists and answered 1) a generic quality of life questionnaire--the Psychological General Well-Being Index (PGWB), 2) a specific function and symptom questionnaire, and 3) a pain questionnaire--the Regional Pain Score (RPS). The same evaluation was repeated at the end of the treatment period. Severity of the condition was assessed by a composite outcome score, a combination of different clinical outcome measures forming a clinical severity index. The variations between these questionnaire scores before and after treatment and the variations between the clinical severity indices estimated by clinicians were used as measures of the treatment impact. The first rationale for the validation was a positive correlation between clinical and questionnaire score changes. Another rationale for validation of the new instruments was the ability to identify the different treatment interventions. RESULTS: The correlation between the clinical severity index and the RPS was good (r = 0.62). Moreover, the RPS demonstrated a good discriminant power in detecting patients with effective treatment: it showed a specificity of 74% and a sensitivity of 75%. The PGWB correlated less well with the clinical score and was less discriminant. The specific function and symptom questionnaire showed little additional validity. CONCLUSIONS: Outcomes of syndrome severity such as pain and subjective well-being, as measured by self-reported questionnaires, can be valid instruments to evaluate treatment efficacy in short-term clinical trials. In the current study, the RPS proved to be particularly useful to assess the widespread tenderness of fibromyalgia and demonstrated high discriminative power.


Subject(s)
Acupuncture Analgesia , Fibromyalgia/diagnosis , Fibromyalgia/therapy , Surveys and Questionnaires/standards , Activities of Daily Living , Adult , Discriminant Analysis , Electroacupuncture , Female , Humans , Male , Middle Aged , Pain Measurement , Reproducibility of Results , Sensitivity and Specificity , Severity of Illness Index , Treatment Outcome
5.
BMJ ; 305(6864): 1249-52, 1992 Nov 21.
Article in English | MEDLINE | ID: mdl-1477566

ABSTRACT

OBJECTIVE: To determine the efficacy of electroacupuncture in patients with fibromyalgia, a syndrome of unknown origin causing diffuse musculoskeletal pain. DESIGN: Three weeks' randomised study with blinded patients and evaluating physician. SETTING: University divisions of physical medicine and rehabilitation and rheumatology, Geneva. PATIENTS: 70 patients (54 women) referred to the division for fibromyalgia as defined by the American College of Rheumatology. INTERVENTIONS: Patients were randomised to electroacupuncture (n = 36) or a sham procedure (n = 34) by means of an electronic numbers generator. MAIN OUTCOME MEASURES: Pain threshold, number of analgesic tablets used, regional pain score, pain recorded on visual analogue scale, sleep quality, morning stiffness, and patient's and evaluating physician's appreciation. RESULTS: Seven of the eight outcome parameters showed a significant improvement in the active treatment group whereas none were improved in the sham treatment group. Differences between the groups were significant for five of the eight outcome measures after treatment. CONCLUSIONS: Electroacupuncture is effective in relieving symptoms of fibromyalgia. Its potential in long term management should now be studied.


Subject(s)
Electroacupuncture , Fibromyalgia/therapy , Adult , Female , Humans , Male , Pain Threshold , Prospective Studies , Treatment Outcome
7.
J Investig Allergol Clin Immunol ; 1(1): 53-7, 1991 Feb.
Article in English | MEDLINE | ID: mdl-1669566

ABSTRACT

Most allergic reactions to fruits and vegetables are immediate IgE-mediated reactions following either contact or ingestion. In such problems, the practice of skin tests represents an important diagnostic tool. However, we often observe a discordance between the clinic and the results of the skin tests performed with commercial glycerinated extracts. A simple procedure of lyophilization applied to some fruits and vegetables is described, which allowed the comparison with fresh juicy material and commercial extracts. This material was applied in 10 individuals shown to be allergic to the corresponding food and in 10 healthy controls. When compared to the commercial extracts, the lyophilized material showed a significantly better sensitivity and specificity. Some control individuals reacted, but insignificantly, to the lyophilized material. The technical procedure is very simple. It allows the preparation of large amounts of aliquot, kept at -20 degrees C until needed. Further work is needed to extend the procedure to other allergens and to improve the standardization.


Subject(s)
Food Hypersensitivity/diagnosis , Fruit/immunology , Skin Tests , Vegetables/immunology , Adolescent , Adult , Aged , Allergens/isolation & purification , Evaluation Studies as Topic , Female , Food Hypersensitivity/immunology , Freeze Drying , Humans , Male , Middle Aged , Radioallergosorbent Test , Sensitivity and Specificity , Skin Tests/statistics & numerical data
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