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1.
Pediatr Rheumatol Online J ; 16(1): 40, 2018 Jun 25.
Article in English | MEDLINE | ID: mdl-29940960

ABSTRACT

BACKGROUND: Juvenile dermatomyositis (JDM) is the most common inflammatory myopathy in childhood and a major cause of morbidity among children with pediatric rheumatic diseases. The management of JDM is very heterogeneous. The JDM working group of the Society for Pediatric Rheumatology (GKJR) aims to define consensus- and practice-based strategies in order to harmonize diagnosis, treatment and monitoring of JDM. METHODS: The JDM working group was established in 2015 consisting of 23 pediatric rheumatologists, pediatric neurologists and dermatologists with expertise in the management of JDM. Current practice patterns of management in JDM had previously been identified via an online survey among pediatric rheumatologists and neurologists. Using a consensus process consisting of online surveys and a face-to-face consensus conference statements were defined regarding the diagnosis, treatment and monitoring of JDM. During the conference consensus was achieved via nominal group technique. Voting took place using an electronic audience response system, and at least 80% consensus was required for individual statements. RESULTS: Overall 10 individual statements were developed, finally reaching a consensus of 92 to 100% regarding (1) establishing a diagnosis, (2) case definitions for the application of the strategies (moderate and severe JDM), (3) initial diagnostic testing, (4) monitoring and documentation, (5) treatment targets within the context of a treat-to-target strategy, (6) supportive therapies, (7) explicit definition of a treat-to-target strategy, (8) various glucocorticoid regimens, including intermittent intravenous methylprednisolone pulse and high-dose oral glucocorticoid therapies with tapering, (9) initial glucocorticoid-sparing therapy and (10) management of refractory disease. CONCLUSION: Using a consensus process among JDM experts, statements regarding the management of JDM were defined. These statements and the strategies aid in the management of patients with moderate and severe JDM.


Subject(s)
Dermatomyositis/drug therapy , Antirheumatic Agents/therapeutic use , Austria , Child , Consensus , Dermatomyositis/diagnosis , Disease Management , Germany , Glucocorticoids/therapeutic use , Humans , Surveys and Questionnaires
3.
Dermatol Surg ; 35(4): 586-92, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19309347

ABSTRACT

BACKGROUND: Photodynamic therapy (PDT) is an effective treatment for actinic keratoses (AKs). Light-emitting diodes (LEDs) offer practical advantages when treating multiple lesions. OBJECTIVE: To evaluate the efficacy and tolerability of PDT using a LED and topical methyl aminolevulinate (MAL) for treatment of multiple AKs. METHODS AND MATERIALS: One hundred thirty-one patients with four to 10 non-pigmented, previously untreated thin or moderately thick AKs on the face or scalp were enrolled in this multicenter, double-blind, randomized, placebo-controlled study. MAL or matching placebo cream was applied to the débrided lesion surface for 3 hours before illumination with noncoherent red light (630 nm, light dose 37 J/cm(2)). Treatment was repeated 1 week later. RESULTS: Efficacy was evaluated in 57 patients with 418 lesions treated with MAL PDT and 58 with 414 lesions treated with placebo PDT. Sixteen patients were excluded as protocol violators (not randomized). MAL PDT was superior (p< .001) to placebo PDT in lesion complete response rates (83.3%, 95% confidence interval (CI)=79.3-86.7%, vs 28.7%, 95% CI=24.4-33.4%) and patient complete response rates (all lesions showing complete response; 68.4%, 95% CI=54.8-80.1% vs 6.9%, 95% CI=1.9-16.7%). CONCLUSIONS: Topical MAL PDT using a LED is an effective treatment for multiple AKs.


Subject(s)
Aminolevulinic Acid/analogs & derivatives , Keratosis, Actinic/drug therapy , Photochemotherapy , Photosensitizing Agents/administration & dosage , Administration, Topical , Adult , Aged , Aged, 80 and over , Aminolevulinic Acid/administration & dosage , Double-Blind Method , Female , Humans , Male , Middle Aged , Photochemotherapy/methods , Treatment Outcome
4.
MMW Fortschr Med ; 149(20): 32-5, 2007 May 17.
Article in German | MEDLINE | ID: mdl-18062134

ABSTRACT

If UV injury of the skin is to be avoided, sun protection by clothing and sunscreen according to the skin type must be employed. Protection against insect stings and bites is provided not only by clothing and mosquito nets but also by suitable repellants, which will depend on the place visited and the user's age.


Subject(s)
Insect Repellents/administration & dosage , Sunburn/prevention & control , Sunscreening Agents/administration & dosage , Travel , Tropical Climate , Ultraviolet Rays/adverse effects , Adolescent , Adult , Age Factors , Child , Female , Humans , Infant , Male , Pregnancy , Protective Clothing , Radiation Effects , Skin/radiation effects , Skin Neoplasms/prevention & control , Sunburn/etiology
5.
Am J Clin Dermatol ; 4(6): 399-406, 2003.
Article in English | MEDLINE | ID: mdl-12762832

ABSTRACT

Optimal management of patients with polymorphous light eruption (PLE), the most frequent photodermatosis, requires knowledge of the individual clinical course of the disease and pathogenic factors. As PLE often causes problems during leisure-time activities and holidays, resulting in a substantial loss of quality of life, prophylaxis is the most important therapeutic approach. Management of PLE must, therefore, focus on basic preventative measures and additional therapeutic approaches, depending on the clinical condition. PLE can be classified into four severity groups (mild, moderate-to-severe, severe and therapy-resistant), which are useful for determining appropriate prophylactic measurements. No specific laboratory tests are available for the diagnosis of PLE, therefore, a clinician must rely on the clinical appearance of the disorder (e.g. clinical symptoms, the location of the lesions, the relationship of the occurrence of the lesions with sun exposure and the time course of the lesions) as well as a patient's medical history in order to make a diagnosis. Basic preventative management of PLE consists of adequate sun protection comprising avoidance of sun exposure, the use of textile sun protection and the application of broadband sunscreens with high UVA protection potential. Other supportive measurements have to be managed individually and are dependent on the patient's medical history and the severity of the disease. Topical antioxidants, systemic immunomodulation, photo(chemo)therapy and systemic immunosuppression may be required in some cases of PLE. Topical antioxidants represent a new treatment approach for moderate-to-severe PLE and are an effective and well tolerated option for this patient population. Severe PLE also requires photo(chemo)therapy. Phototherapy can be in the form of 311 nm UVB or UVA1 irradiation. In cases where 311 nm UVB or UVA1 are ineffective, psoralen plus UVA (PUVA) bath therapy may be used. However, PUVA bath therapy must be used with caution because it is associated with acute and long-term adverse effects. In rare exceptions we would consider using oral PUVA therapy. However, in our outpatient department, quality of life of most patients is improved with the treatment regimens that are recommended for patients with moderate-to-severe PLE, without the need for photo(chemo)therapy.


Subject(s)
Dermatitis, Photoallergic/therapy , Administration, Topical , Antioxidants/therapeutic use , Dermatitis, Photoallergic/diagnosis , Dermatitis, Photoallergic/physiopathology , Histamine H1 Antagonists/therapeutic use , Humans , Immunosuppressive Agents/therapeutic use , Photochemotherapy , Sunscreening Agents/therapeutic use
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