Outcomes assessment with two different medication administration modalities for the treatment of secondary hyperparathyroidism

Bibliographic Details
Main Author: Pinto,Jose Reimao
Publication Date: 2013
Other Authors: Ponce,Pedro
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692013000400008
Summary: Background: The treatment of hyperparathyroidism in dialysis patients relies on adequate control of serum phosphorus (Pi) and PTH levels. Patient (pt) compliance to oral therapy at home is known to be quite poor and cannot be monitored. There is evidence that pulse (every other day) therapy with vitamin D compounds is as effective as daily administration. We hypothesized that the same might apply to calcimimetics. Objective: To assess the effect on metabolic endpoints of changing cinacalcet oral treatment from a daily, home-based administration (H), to a three-times/week witnessed administration at the end of each dialysis session in the clinic (C). Patient and methods: 93 prevalent dialysis pts in 6 clinics were included in an observational retrospective study, each patient serving as his own historical control. Inclusion criteria were: ESRD treated by haemodialysis; PTH levels &gt; 500 ng/L and cinacalcet prescription for more than 9 months. Data was drawn from a database common to all participating clinics - EuCliDc. Blood samples were collected at the beginning of dialysis and treated at a central laboratory. Calcium (Ca), phosphorus, albumin and PTH were registered every 3 months, as well as vitamin D and cinacalcet dosages, in the last 9 months of period H and first 9 months of period C. Values during H prescription were compared with values after change to C administration through paired samples t-test. Results: We detected a significant reduction in the dose of Cinacalcet from an average dose of 1221mg/month in period H to an average dose of 674.4mg/month in period C, p < 0.0001 (95% CI 689.4 / 405.1), keeping identical dosages of Vitamin D metabolite 21.3 mic/month vs. 31.9mic/month, p=.167. This dose reduction was translated, as expected, in cost savings, going from an average Cinacalcet cost of 256€/month/pt to 137.6€/month/patient, p < 0.0001. PTH was more elevated in the C group 903.5 vs. 807.9ng/L, < 0.028, phosphate levels were identical, 5.0 in period H and 4.8mg/dl in period C, p = 0.065. Conclusion: Administration of Cinacalcet under supervision 3 times per week, post -dialysis, was shown to be safe, guarantees compliance and saved considerable resources for the same therapeutic efficacy.
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spelling Outcomes assessment with two different medication administration modalities for the treatment of secondary hyperparathyroidismCinacalcetcompliancehaemodialysishyperparathyroidismBackground: The treatment of hyperparathyroidism in dialysis patients relies on adequate control of serum phosphorus (Pi) and PTH levels. Patient (pt) compliance to oral therapy at home is known to be quite poor and cannot be monitored. There is evidence that pulse (every other day) therapy with vitamin D compounds is as effective as daily administration. We hypothesized that the same might apply to calcimimetics. Objective: To assess the effect on metabolic endpoints of changing cinacalcet oral treatment from a daily, home-based administration (H), to a three-times/week witnessed administration at the end of each dialysis session in the clinic (C). Patient and methods: 93 prevalent dialysis pts in 6 clinics were included in an observational retrospective study, each patient serving as his own historical control. Inclusion criteria were: ESRD treated by haemodialysis; PTH levels &gt; 500 ng/L and cinacalcet prescription for more than 9 months. Data was drawn from a database common to all participating clinics - EuCliDc. Blood samples were collected at the beginning of dialysis and treated at a central laboratory. Calcium (Ca), phosphorus, albumin and PTH were registered every 3 months, as well as vitamin D and cinacalcet dosages, in the last 9 months of period H and first 9 months of period C. Values during H prescription were compared with values after change to C administration through paired samples t-test. Results: We detected a significant reduction in the dose of Cinacalcet from an average dose of 1221mg/month in period H to an average dose of 674.4mg/month in period C, p < 0.0001 (95% CI 689.4 / 405.1), keeping identical dosages of Vitamin D metabolite 21.3 mic/month vs. 31.9mic/month, p=.167. This dose reduction was translated, as expected, in cost savings, going from an average Cinacalcet cost of 256€/month/pt to 137.6€/month/patient, p < 0.0001. PTH was more elevated in the C group 903.5 vs. 807.9ng/L, < 0.028, phosphate levels were identical, 5.0 in period H and 4.8mg/dl in period C, p = 0.065. Conclusion: Administration of Cinacalcet under supervision 3 times per week, post -dialysis, was shown to be safe, guarantees compliance and saved considerable resources for the same therapeutic efficacy.Sociedade Portuguesa de Nefrologia2013-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articletext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692013000400008Portuguese Journal of Nephrology &amp; Hypertension v.27 n.4 2013reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAPenghttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692013000400008Pinto,Jose ReimaoPonce,Pedroinfo:eu-repo/semantics/openAccess2024-02-06T17:04:43Zoai:scielo:S0872-01692013000400008Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T12:54:22.174623Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Outcomes assessment with two different medication administration modalities for the treatment of secondary hyperparathyroidism
title Outcomes assessment with two different medication administration modalities for the treatment of secondary hyperparathyroidism
spellingShingle Outcomes assessment with two different medication administration modalities for the treatment of secondary hyperparathyroidism
Pinto,Jose Reimao
Cinacalcet
compliance
haemodialysis
hyperparathyroidism
title_short Outcomes assessment with two different medication administration modalities for the treatment of secondary hyperparathyroidism
title_full Outcomes assessment with two different medication administration modalities for the treatment of secondary hyperparathyroidism
title_fullStr Outcomes assessment with two different medication administration modalities for the treatment of secondary hyperparathyroidism
title_full_unstemmed Outcomes assessment with two different medication administration modalities for the treatment of secondary hyperparathyroidism
title_sort Outcomes assessment with two different medication administration modalities for the treatment of secondary hyperparathyroidism
author Pinto,Jose Reimao
author_facet Pinto,Jose Reimao
Ponce,Pedro
author_role author
author2 Ponce,Pedro
author2_role author
dc.contributor.author.fl_str_mv Pinto,Jose Reimao
Ponce,Pedro
dc.subject.por.fl_str_mv Cinacalcet
compliance
haemodialysis
hyperparathyroidism
topic Cinacalcet
compliance
haemodialysis
hyperparathyroidism
description Background: The treatment of hyperparathyroidism in dialysis patients relies on adequate control of serum phosphorus (Pi) and PTH levels. Patient (pt) compliance to oral therapy at home is known to be quite poor and cannot be monitored. There is evidence that pulse (every other day) therapy with vitamin D compounds is as effective as daily administration. We hypothesized that the same might apply to calcimimetics. Objective: To assess the effect on metabolic endpoints of changing cinacalcet oral treatment from a daily, home-based administration (H), to a three-times/week witnessed administration at the end of each dialysis session in the clinic (C). Patient and methods: 93 prevalent dialysis pts in 6 clinics were included in an observational retrospective study, each patient serving as his own historical control. Inclusion criteria were: ESRD treated by haemodialysis; PTH levels &gt; 500 ng/L and cinacalcet prescription for more than 9 months. Data was drawn from a database common to all participating clinics - EuCliDc. Blood samples were collected at the beginning of dialysis and treated at a central laboratory. Calcium (Ca), phosphorus, albumin and PTH were registered every 3 months, as well as vitamin D and cinacalcet dosages, in the last 9 months of period H and first 9 months of period C. Values during H prescription were compared with values after change to C administration through paired samples t-test. Results: We detected a significant reduction in the dose of Cinacalcet from an average dose of 1221mg/month in period H to an average dose of 674.4mg/month in period C, p < 0.0001 (95% CI 689.4 / 405.1), keeping identical dosages of Vitamin D metabolite 21.3 mic/month vs. 31.9mic/month, p=.167. This dose reduction was translated, as expected, in cost savings, going from an average Cinacalcet cost of 256€/month/pt to 137.6€/month/patient, p < 0.0001. PTH was more elevated in the C group 903.5 vs. 807.9ng/L, < 0.028, phosphate levels were identical, 5.0 in period H and 4.8mg/dl in period C, p = 0.065. Conclusion: Administration of Cinacalcet under supervision 3 times per week, post -dialysis, was shown to be safe, guarantees compliance and saved considerable resources for the same therapeutic efficacy.
publishDate 2013
dc.date.none.fl_str_mv 2013-12-01
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dc.publisher.none.fl_str_mv Sociedade Portuguesa de Nefrologia
publisher.none.fl_str_mv Sociedade Portuguesa de Nefrologia
dc.source.none.fl_str_mv Portuguese Journal of Nephrology &amp; Hypertension v.27 n.4 2013
reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron:RCAAP
instname_str FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron_str RCAAP
institution RCAAP
reponame_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
collection Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
repository.name.fl_str_mv Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
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