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1.
Ultraschall Med ; 25(2): 131-6, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15085455

ABSTRACT

OBJECTIVE: We report on a 3-year experience using single-shot, ultrasonography-guided, percutaneous ethanol ablation (PEA) of hyperplastic parathyroid glands in chronic dialysis patients suffering from secondary or tertiary hyperparathyroidism. MATERIALS AND METHODS: Seventeen uraemic patients (mean age 52 +/- 14 years) with hypercalcaemia and elevated serum levels of parathyroid hormone were assessed for ethanol ablation. Ten patients did not fulfil the inclusion criteria and underwent surgical parathyroidectomy. Seven patients were treated using PEA. RESULTS: All patients treated with PEA tolerated the procedure well, and no major complications were observed. Three out of seven patients underwent further ethanol ablation due to recurrent symptomatic hyperparathyroidism. Following the procedures, serum values of total calcium and parathyroid hormone remained within target range with concomitant medical therapy in all patients. CONCLUSION: PEA performed as a single-shot therapy can be used as a minimally invasive and safe supplement to medical therapy in the treatment of secondary or tertiary hyperparathyroidism in selected patients. In case of recurrence, treatment can be repeated without any problems.


Subject(s)
Catheter Ablation/methods , Hyperparathyroidism/etiology , Renal Dialysis/adverse effects , Uremia/therapy , Adult , Aged , Ethanol , Female , Humans , Hyperparathyroidism/diagnostic imaging , Hyperparathyroidism/pathology , Hyperparathyroidism/therapy , Hyperparathyroidism, Secondary/diagnostic imaging , Hyperparathyroidism, Secondary/etiology , Hyperparathyroidism, Secondary/pathology , Hyperparathyroidism, Secondary/therapy , Hyperplasia , Male , Middle Aged , Monitoring, Physiologic/methods , Parathyroid Glands/anatomy & histology , Parathyroid Glands/diagnostic imaging , Safety , Ultrasonography
2.
J Hepatol ; 11 Suppl 1: S50-3, 1990.
Article in English | MEDLINE | ID: mdl-2127788

ABSTRACT

Thirty patients with chronic non-A, non-B hepatitis (24 male, six female; median age 38 years, range: 15-68 years) were treated with recombinant interferon alfa-2b for 1 year. Treatment was started with 5 million units interferon alfa-2b daily for 2 weeks followed by 2 million units daily for another 2 weeks. Further doses were titrated according to alanine aminotransferase values. After 1 year, treatment was stopped and a follow-up biopsy was obtained. Thereafter, patients were followed for 6 months. Of the 24 patients who completed the 1-year treatment period, 14 (58%) had normal alanine aminotransferase values at the end of the study, eight of whom showed transient increases while on treatment. In another seven (29%), alanine aminotransferase levels decreased by more than 50% of pre-treatment values but remained above the normal range. Biopsies at the end of treatment showed a complete disappearance of inflammatory activity in four and a marked improvement in eleven other patients. The results of this study indicate that a 1-year treatment with recombinant interferon alfa-2b of patients with non-A, non-B hepatitis was very effective at normalizing or improving serum transaminases and liver histology. However, the overall relapse rate was 57%, with relapse occurring in a greater proportion of patients with temporary breakthroughs during therapy (requiring dosage increase), and particularly of patients with only a partial response to treatment (serum transaminases decreased by greater than or equal to 50%). Thus, further studies are needed to establish the optimal dose and duration of treatment to induce a complete resolution of the disease.


Subject(s)
Hepatitis C/therapy , Interferon-alpha/therapeutic use , Adult , Alanine Transaminase/analysis , Biomarkers/blood , Chronic Disease , Female , Hepatitis C/blood , Hepatitis C/pathology , Humans , Interferon alpha-2 , Liver/pathology , Male , Recombinant Proteins
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