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P1426EFFECTIVENESS AND SAFETY OF ETELCALCETIDE IN THE LONG TERM IN CLINICAL PRACTICE IN HEMODIALYSIS PATIENTS WITH SECONDARY HYPERPARATHYROIDISM
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Abstract
Background and Aims
: Secondary hyperparathyroidism (HPT) is a frequent complication in hemodialysis (HD) patients. Until now we had oral Vit / D analogues and oral Cinacalcet for treatment. The appearance of Etelcalcetide brings new treatment possibilities. Apart from clinical trials there are few long-term results in usual practice. Our goal is to evaluate results with the use of Etelcalcetide after more than a year of treatment in clinical practice of HD.
Method
We carry out a prospective descriptive study for 15 months with patients with HPT-HD, the ones who were with Cinacalcet and had not responded or had intolerance were changed to Etelcalcetide. Patients without prior treatment with calcimimetics were also included. Treatment with Vit D analogues and phosphate binders is treated according to usual clinical practice.
Results
We studied 25 HD patients, 12 men and 13 women with a mean age of 59.5 ± 13.6 years, 11 began de novo calcimimetic treatment and in 14 Cinacalcet was modified to Etelcalcetide due to lack of response or poor oral tolerance. Starting dose 2.5 mg post-dialysis, mean final dose 7.5 mg. We observed a reduction of PTH ≥30% in 80% of patients and a decrease ≥50% in 52%, Figure 1 shows the decrease over 15 months. The calcium corrected to albumine (Cac) decreased 4.8% ± 8 compared to baseline. The majority of patients present mild hypocalcemia (Cac between 7.5 and 8.3 mg / dl) and asymptomatic. There are no differences with P. Patients with PTH in range according to KDIGO went from 8% to 63%. No serious clinical manifestations of hypocalcemia or symptoms of digestive intolerance or other side effects appeared.
Conclusion
Etelcalcetide in the long term significantly improves the control of HPT in HD with a high safety profile. IV administration facilitates compliance without having followed serious side effects in 15 months of follow-up.
Oxford University Press (OUP)
Title: P1426EFFECTIVENESS AND SAFETY OF ETELCALCETIDE IN THE LONG TERM IN CLINICAL PRACTICE IN HEMODIALYSIS PATIENTS WITH SECONDARY HYPERPARATHYROIDISM
Description:
Abstract
Background and Aims
: Secondary hyperparathyroidism (HPT) is a frequent complication in hemodialysis (HD) patients.
Until now we had oral Vit / D analogues and oral Cinacalcet for treatment.
The appearance of Etelcalcetide brings new treatment possibilities.
Apart from clinical trials there are few long-term results in usual practice.
Our goal is to evaluate results with the use of Etelcalcetide after more than a year of treatment in clinical practice of HD.
Method
We carry out a prospective descriptive study for 15 months with patients with HPT-HD, the ones who were with Cinacalcet and had not responded or had intolerance were changed to Etelcalcetide.
Patients without prior treatment with calcimimetics were also included.
Treatment with Vit D analogues and phosphate binders is treated according to usual clinical practice.
Results
We studied 25 HD patients, 12 men and 13 women with a mean age of 59.
5 ± 13.
6 years, 11 began de novo calcimimetic treatment and in 14 Cinacalcet was modified to Etelcalcetide due to lack of response or poor oral tolerance.
Starting dose 2.
5 mg post-dialysis, mean final dose 7.
5 mg.
We observed a reduction of PTH ≥30% in 80% of patients and a decrease ≥50% in 52%, Figure 1 shows the decrease over 15 months.
The calcium corrected to albumine (Cac) decreased 4.
8% ± 8 compared to baseline.
The majority of patients present mild hypocalcemia (Cac between 7.
5 and 8.
3 mg / dl) and asymptomatic.
There are no differences with P.
Patients with PTH in range according to KDIGO went from 8% to 63%.
No serious clinical manifestations of hypocalcemia or symptoms of digestive intolerance or other side effects appeared.
Conclusion
Etelcalcetide in the long term significantly improves the control of HPT in HD with a high safety profile.
IV administration facilitates compliance without having followed serious side effects in 15 months of follow-up.
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