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1.
Clin Exp Allergy ; 39(1): 116-26, 2009 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-19137651

RESUMO

BACKGROUND: The remission rate of patients with chronic urticaria (CU) due to elimination diets varies between 31% and 71%. However, the diagnostic value of subsequent traditional oral provocation tests with food additives in capsules remains unsatisfactory. OBJECTIVES: A newly incremental build-up food challenge (IBUF) for patients with CU was designed and implemented in an open pilot study. Primary endpoint was the percentage of patients developing urticaria during at least one step of IBUF after an initial complete remission due to a pseudoallergen-free elimination diet. METHODS: In total, 153 patients with CU were submitted for 5 weeks to a pseudoallergen-free diet. All patients with remission were included to the 6-week IBUF protocol, containing pseudoallergen-rich foods in a systematic and additive manner. The recurrence and severity of CU was evaluated by urticaria score. Subjective disturbance and quality of life were evaluated by patients' diary, visual analogue scale and quality of life questionnaire (CU-Q2oL). Subsequently, patients were followed up for 3-24 months after IBUF by a telephone interview. RESULTS: A total of 104 patients completed the pseudoallergen-free diet, whereby 51% reported partial, 17% complete and 32% no remission due to the diet. All diet responders showed a decrease in subjective impairment, urticaria and quality of life score (P<0.001 each). Eighty-six percent (12/14) of the patients reaching complete remission, showed a recurrence of urticaria symptoms during the IBUF protocol. Fifty-eight percent (7/12) of these patients still remained free of symptoms due to avoidance of IBUF-identified foods at telephone follow-up. In patients with partial remission to pseudoallergen-free diet, however, IBUF did not provide information about the cause of urticaria symptoms. CONCLUSIONS: The newly developed IBUF protocol seemed to be a promising method for identifying individually incompatible foods in some CU patients. IBUF should be verified by randomized controlled trials to gain additional evidence for its diagnostic value.


Assuntos
Alérgenos , Aditivos Alimentares , Hipersensibilidade Alimentar/dietoterapia , Urticária/dietoterapia , Adolescente , Adulto , Idoso , Alérgenos/administração & dosagem , Alérgenos/efeitos adversos , Alérgenos/imunologia , Criança , Doença Crônica , Feminino , Aditivos Alimentares/administração & dosagem , Aditivos Alimentares/efeitos adversos , Humanos , Masculino , Pessoa de Meia-Idade , Projetos Piloto , Qualidade de Vida , Recidiva , Índice de Gravidade de Doença , Urticária/imunologia , Urticária/fisiopatologia , Adulto Jovem
2.
J Eur Acad Dermatol Venereol ; 21(1): 90-4, 2007 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17207174

RESUMO

BACKGROUND AND OBJECTIVE: Pimecrolimus cream 1% is an effective treatment for atopic eczema. The aim was to investigate its efficacy in asteatotic eczema, a skin disease similar to atopic eczema and its associated dry skin and itching. METHODS: Single-centre, randomized, double-blind, vehicle controlled study in 40 patients with asteatotic eczema. Efficacy was assessed by eczema area and severity index (EASI), investigators global assessment (IGA), patient's self-assessment, and pruritus severity. RESULTS: After 4 weeks of treatment, EASI, the primary efficacy variable, was reduced by 62+/-7% from baseline in patients on pimecrolimus, compared to 21+/-14% in patients on vehicle (P=0.013). With pimecrolimus there was also a better control of pruritus (P=0.042) at week 4 whereas a better control of disease according to self-assessment could only be observed at weeks 2 (P=0.01) and week 3 (P=0.08). CONCLUSION: Pimecrolimus cream 1% is effective in patients with asteatotic eczema.


Assuntos
Fármacos Dermatológicos/uso terapêutico , Eczema/tratamento farmacológico , Tacrolimo/análogos & derivados , Adulto , Fármacos Dermatológicos/administração & dosagem , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Veículos Farmacêuticos , Tacrolimo/administração & dosagem , Tacrolimo/uso terapêutico
3.
Hautarzt ; 57(9): 785-91, 2006 Sep.
Artigo em Alemão | MEDLINE | ID: mdl-16240154

RESUMO

The rapid increase of atopic diseases, particularly in western industrialized countries, demands comprehensive and cost-effective primary prevention. Existing findings regarding the use of probiotic lactic acid bacteria for the prevention of atopic eczema are promising. Therapeutic use appears to be more promising for infants with mild to moderate skin lesions and elevated immunoglobulin E levels than for older patients without any sensitization. Depending on the original bacterial count, prebiotics such as fructooligosaccharides and galactooligosaccharides cause an increase of bifidobacteria within the colon. The benefit of this increase in bifidobacteria in allergic diseases is unclear. In patients with atopic eczema a correlation was shown between the amount of bifidobacteria and the severity of atopic eczema.


Assuntos
Dermatite Atópica/microbiologia , Dermatite Atópica/terapia , Lactobacillus , Probióticos/uso terapêutico , Dermatite Atópica/prevenção & controle , Humanos , Guias de Prática Clínica como Assunto , Padrões de Prática Médica/tendências , Resultado do Tratamento
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