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1.
J Dermatolog Treat ; 33(3): 1397-1400, 2022 May.
Artigo em Inglês | MEDLINE | ID: mdl-32885699

RESUMO

INTRODUCTION: There is scarcity of prospective studies assessing the correlation between vitamin D deficiency and atopic dermatitis (AD). MATERIALS AND METHODS: We conducted a prospective study where in serum 25-hydroxy-vitamin D levels were measured in 35 AD patients and 35 age and sex-matched controls. AD patients deficient in vitamin D were supplemented with 1000 IU of vitamin D per day for three months. Serum vitamin D levels and SCORAD were again measured at the end of three months in all AD patients. RESULTS: The baseline vitamin D levels in patients and controls did not have any statistically significant difference (p = .97). There was a statistically significant (p = .02) inverse relationship between the AD severity and serum vitamin D levels at baseline (r = -0.52). Maximum reduction in SCORAD (41.4 ± 12.7) after 3 months of vitamin D supplementation was seen in severe AD and the minimum (2.4 ± 13.2) in mild AD (p = .0003). CONCLUSIONS: We found no difference in the mean serum vitamin D levels between AD patients and controls. An inverse correlation was seen between serum vitamin D levels at baseline and severity of AD. Beneficial effect of vitamin D supplementation was observed maximally in severe AD as observed by a reduction in SCORAD.


Assuntos
Dermatite Atópica , Criança , Dermatite Atópica/tratamento farmacológico , Suplementos Nutricionais , Humanos , Estudos Prospectivos , Índice de Gravidade de Doença , Resultado do Tratamento , Vitamina D/uso terapêutico , Vitaminas/uso terapêutico
3.
Indian J Dermatol Venereol Leprol ; 84(2): 174-178, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-28397714

RESUMO

BACKGROUND: The use of glucocorticoids in various forms of administration is complicated by their systemic side effects. Although intravenous pulse therapy is considered to have lesser systemic side effects, there are few studies in literature comparing the effects of intravenous pulse glucocorticoids versus oral daily glucocorticoids on bone mineral density. AIM: To compare the effects of intravenous pulse glucocorticoids and oral daily glucocorticoids on bone mineral density with the aim of finding any site-specific osteopenic side effect. METHODS: The study was conducted by the department of dermatology of Postgraduate Institute of Medical Education and Research, Chandigarh, India. The study comprised of two groups of patients. Group A consisted of 28 patients with pemphigus vulgaris who received intravenous pulses of dexamethasone at 4 weekly intervals. Group B consisted of 21 patients with airborne contact dermatitis who received oral daily prednisolone therapy. All the patients had a dual X-ray absorptiometry scan at baseline, and at 3 and 6 months of follow-up. The results were analyzed as changes in bone mineral density. RESULTS: There was loss of bone mineral density at lumbar spine and the head of radius in both the groups. At the lumbar spine, Group B showed more reduction in bone mineral density at 3 months whereas in Group A it was more at the head of radius. In patients on oral steroids, the lumbar spine was significantly more affected than the head of radius at both 3 and 6 months of follow-up. However, in patients on intravenous pulse steroids, both the sites were equally affected at 3 and 6 months. LIMITATIONS: In our study, we used different glucocorticoids in the two groups: prednisolone in the oral daily group and dexamethasone in the intravenous pulse steroids group. A similar reduction in bone mineral density in both the groups may have been due to a longer half-life or more bone-directed side effects of dexamethasone as compared to prednisolone. CONCLUSION: Dermatologists need to be aware of the detrimental effects of high-dose intravenous pulsed glucocorticoids on bone mineral density and assessment of this parameter should be done before the initiation of therapy and also at regular intervals thereafter. During follow up, either the lumbar spine or the head of radius can be used to assess the osteopenic effect of intravenous pulse steroids, whereas the lumbar spine is a better site for this evaluation in patients on oral steroids.


Assuntos
Anti-Inflamatórios/administração & dosagem , Densidade Óssea/efeitos dos fármacos , Dexametasona/administração & dosagem , Glucocorticoides/administração & dosagem , Prednisolona/administração & dosagem , Dermatopatias/tratamento farmacológico , Administração Intravenosa , Administração Oral , Densidade Óssea/fisiologia , Dermatologia , Feminino , Humanos , Masculino , Pulsoterapia , Dermatopatias/diagnóstico , Resultado do Tratamento
4.
Artigo em Inglês | MEDLINE | ID: mdl-25937142

RESUMO

BACKGROUND: Parthenium hysterophorus is the leading cause of phytogenic allergic contact dermatitis in India. The Indian Standard Series currently supplied by Systopic Laboratories Ltd and manufactured by Chemotechnique Diagnostics ® contains parthenolide as the only allergen representing plant allergens. AIM: The study was conducted to assess the performance of the Chemotechnique plant series (PL-1000), consisting of 14 allergens, in patients with clinically suspected occupational contact dermatitis to plant allergens. METHODS: Ninety patients were patch tested with the Chemotechnique plant series from 2011 to 2013. Demographic details, clinical diagnosis and patch test results were recorded in the contact dermatitis clinic proforma. RESULTS: Of 90 patients, 24 (26.7%) showed positive reactions to one or more allergens in the plant series. Positive patch tests were elicited most commonly by sesquiterpene lactone mix in 19 (78.6%) patients, followed by parthenolide in 14 (57.1%), Achillea millefolium in 10 (42.9%) and others in decreasing order. CONCLUSION: The plant allergen series prepared by Chemotechnique Diagnostics is possibly not optimal for diagnosing suspected allergic contact dermatitis to plants in north Indians. Sesquiterpene lactone mix should replace parthenolide as the plant allergen in the Indian Standard Series until relevant native plant extracts are commercially available for patch testing.


Assuntos
Alérgenos/imunologia , Asteraceae/imunologia , Dermatite Alérgica de Contato/etiologia , Dermatite Ocupacional/etiologia , Plantas/imunologia , Achillea/imunologia , Adulto , Alérgenos/efeitos adversos , Dermatite Alérgica de Contato/diagnóstico , Dermatite Ocupacional/diagnóstico , Feminino , Humanos , Índia , Lactonas/imunologia , Masculino , Pessoa de Meia-Idade , Testes do Emplastro , Plantas/efeitos adversos , Sesquiterpenos/imunologia , Tanacetum/imunologia
6.
Artigo em Inglês | MEDLINE | ID: mdl-21079306

RESUMO

Psoriasis is a common, chronic, inflammatory disease with a wide range of clinical presentations. The disease severity ranges from mild to severe. Plaque type of psoriasis is the most common. A number of factors like previous treatment history and comorbid conditions influence the treatment of psoriasis in an individual patient. Location of the lesions is also an important consideration. Psoriasis localized to certain areas of the body like scalp, nails, palms and soles remains difficult to treat. These sites have been referred to as the difficult locations in literature. This article covers the management of psoriasis limited to these special areas.


Assuntos
Fármacos Dermatológicos/administração & dosagem , Fototerapia/tendências , Psoríase/tratamento farmacológico , Psoríase/patologia , Administração Tópica , Animais , Gerenciamento Clínico , Dermatoses do Pé/tratamento farmacológico , Dermatoses do Pé/patologia , Dermatoses da Mão/tratamento farmacológico , Dermatoses da Mão/patologia , Humanos , Doenças da Unha/tratamento farmacológico , Doenças da Unha/patologia , Fototerapia/métodos , Dermatoses do Couro Cabeludo/tratamento farmacológico , Dermatoses do Couro Cabeludo/patologia
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