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

Detalhes bibliográficos
Autor(a) principal: Pinto,Jose Reimao
Data de Publicação: 2013
Outros Autores: Ponce,Pedro
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692013000400008
Resumo: 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.
id RCAP_63ca9655b06a59d783fdcdeddfe68c17
oai_identifier_str oai:scielo:S0872-01692013000400008
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
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:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron: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/openaireopendoar:71602024-03-20T02:18:51.416331Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
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
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692013000400008
url http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692013000400008
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692013000400008
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
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:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799137278992318464