scholarly journals A single centre retrospective analysis of cinacalcet therapy in primary hyperparathyroidism

2021 ◽  
Author(s):  
Daniel Bell ◽  
Julia Hale ◽  
Cara Go ◽  
Ben George Challis ◽  
Tilak Das ◽  
...  

Primary hyperparathyroidism (pHPT) is a common endocrine disorder that can be cured by parathyroidectomy, and patients unsuitable for surgery can be treated with cinacalcet. Availability of surgery may be reduced during COVID-19 and cinacalcet can be used as bridging therapy. In this single centre retrospective analysis, we investigated the efficacy and safety of cinacalcet in patients with pHPT receiving cinacalcet between March 2019 and July 2020, including pre-parathyroidectomy bridging. We reviewed and summarised the published literature. 86 patients were identified, with most achieving target calcium (79.1%) with a mean dose of 39.4 mg/day for a median duration of 35 weeks. Calcium normalised in a median time of 5 weeks. The majority of patients commenced cinacalcet 30 mg/day (78; 90.7%) with the remainder at 60 mg/day (8; 9.3%). 57.8% of patients commenced on lower dose cinacalcet (30 mg/day) achieved a target Ca without requiring 60 mg/day. Baseline PTH was significantly higher in patients requiring higher doses of cinacalcet (p=0.014). 18.6% of patients reported adverse reactions and 4.7% discontinued cinacalcet. Patients treated with cinacalcet pre-parathyroidectomy required a higher dose and fewer achieved target calcium compared to those treated medically with cinacalcet alone. Post-operative calcium was similar to patients not given pre-parathyroidectomy cinacalcet. In summary, cinacalcet at an initial dose of 30 mg/day is safe and effective for achieving target calcium in patients with symptomatic or severe hypercalcaemia in pHPT, including those treated pre-parathyroidectomy. We propose a PTH threshold of >30 pmol/L to initiate at a higher dose of 60 mg/day.

Author(s):  
L.G. Khludova ◽  
I.A. Manto ◽  
E.A. Latysheva ◽  
T.V. Latysheva ◽  
M.R. Khaitov

Актуальность. Заместительная терапия иммуноглобулинами человека является ведущим патогенетическим методом лечения первичных иммунодефицитов с нарушением синтеза антител. В настоящее время в России доступно несколько препаратов иммуноглобулинов человека нормальных для внутривенного введения. Цель. Оценить эффективность и безопасность препарата Привиджен (10 раствор иммуноглобулина для внутривенного введения) в реальной клинической практике в течение 12 клинических месяцев. Материалы и методы. 20 взрослых с диагнозом общая вариабельная иммунная недостаточности и Х-сцепленная агаммаглобулинемия получали внутривенный иммуноглобулин Привиджен к интервалом 243 дня в течение 12 мес. Первичными критериями оценки была частота инфекционных осложнений и нежелательных явлений. Результаты. У большинства пациентов в ходе исследования достигнут удовлетворительный претранс-фузионный уровень IgG. Тяжелых нежелательных явлений, связанных с введением препарата, не зарегистрировано. Заключение. В ходе исследования препарат продемонстрировал высокую эффективность и безопасность у пациентов, нуждающихся в ежемесячной заместительной терапииRelevance. Replacement therapy with human immunoglobulins is the leading pathogenetic method of treatment of primary immunodeficiency with impaired antibody synthesis. Currently, several preparations of human immunoglobulins for intravenous administration are available in Russia. Purposes. Evaluation of the efficacy and safety of Privigen immunoglobulin intravenous 10 liquid in real clinical practice within 12 clinical months. Methods. Twenty adults diagnosed with common variable immunodeficiency or X-linked agammaglobulinemia received intravenous Privigen infusions (0.2-0.4 mg/kg) at 243 intervals over a 12-month period. The primary endpoint was the annual rate of infections and adverse events. Results. Sufficient level of IgG was achieved in most patients during the study. Severe adverse reactions during the treatment were not registered. Conclusions. High efficacy and safety of monthly replacement therapy in patients with primary immunodeficiency with impaired antibody synthesis has been demonstrated.


2021 ◽  
Vol 32 ◽  
pp. S329
Author(s):  
Koshi Sukeno ◽  
Akira Tsunoda ◽  
Yasutaka Tono ◽  
Hiroyasu Oda ◽  
Mikiya Ishihara ◽  
...  

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