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Efficacy and safety of combined parenteral and oral steroid therapy in Graves' orbitopathy.
Nedeljkovic Beleslin, Biljana; Ciric, Jasmina; Zarkovic, Milos; Stojkovic, Mirjana; Savic, Slavica; Knezevic, Miroslav; Stankovic, Branislav; Trbojevic, Bozo.
Afiliação
  • Nedeljkovic Beleslin B; Clinic for Endocrinology, Diabetes and Metabolic Disorders, Clinical Center of Serbia; Medical School, University of Belgrade; Serbia.
  • Ciric J; Clinic for Endocrinology, Diabetes and Metabolic Disorders, Clinical Center of Serbia; Medical School, University of Belgrade; Serbia.
  • Zarkovic M; Clinic for Endocrinology, Diabetes and Metabolic Disorders, Clinical Center of Serbia; Medical School, University of Belgrade; Serbia.
  • Stojkovic M; Clinic for Endocrinology, Diabetes and Metabolic Disorders, Clinical Center of Serbia; Belgrade; Serbia.
  • Savic S; Clinic for Endocrinology, Diabetes and Metabolic Disorders, Clinical Center of Serbia; Belgrade; Serbia.
  • Knezevic M; Medical School, University of Belgrade; Clinic for Ophthalmology, Clinical Center of Serbia; Belgrade, Serbia.
  • Stankovic B; Medical School, University of Belgrade; Clinic for Ophthalmology, Clinical Center of Serbia; Belgrade, Serbia.
  • Trbojevic B; Clinic for Endocrinology, Diabetes and Metabolic Disorders, Clinical Center of Serbia; Medical School, University of Belgrade; Serbia.
Hormones (Athens) ; 13(2): 222-8, 2014.
Article em En | MEDLINE | ID: mdl-24776622
OBJECTIVE: Glucocorticoids (GC) are the treatment of choice for moderate-to-severe and active Graves' orbitopathy (GO), but optimal treatment is still . The aim of the present study was to analyze the efficacy and tolerability of combined parenteral GC pulse therapy followed by oral GC in the interpulse period. DESIGN: The study included 50 patients (48 ± 10 years; 37 female) with untreated, active and moderate-to-severe GO. Patients received 500 mg of methylprednisolone in 500 ml of physiologic saline. Infusion was repeated after 48 h and then followed by tapering doses of oral prednisone and the cycle repeated each month for the next 5 months. The cumulative dose was 10.2g.Ophthalmic assessment was performed before and 6 months after start of treatment. Side effects of GC therapy were evaluated and recorded each month. RESULTS: GC showed the greatest effectiveness on soft tissue changes (incorporated in the CAS). Median CAS values decreased from 4.5 to 2 (p>0.001). Improvement was demonstrated in 37 patients (74%), there was no change in 13 patients (26%) and none of the patients presented with deterioration of inflammatory status. Diplopia improved in 21 patients (42%), was unchanged in 28 patients (56%) and deteriorated in 1 patient (2%). Improvement in visual acuity occurred in 36% of patients. At 6 months, 33/50 patients (66%) demonstrated overall treatment response. Response to GC therapy was influenced by CAS, TSHRAb and smoking behavior. The only independent parameter associated with positive treatment response was CAS ≥ 4 (p<0.001). Side effects occurred in 35/50 patients (70%) and the vast majority of them were mild to moderate. During the 6-months follow-up period, 2/33 patients (6%) had relapsing GO. CONCLUSION: With appropriate selection of patients and careful monitoring during and after treatment, combined parenteral and oral GC therapy is effective and safe.
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Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article