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1.
Am J Kidney Dis ; 70(5): 696-704, 2017 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-28838766

RESUMO

BACKGROUND: Low concentrations and excessive concentrations of trace elements have been commonly reported in hemodialysis patients, but available studies have several important limitations. STUDY DESIGN: Random sample of patients drawn from a prospective cohort. SETTING & PARTICIPANTS: 198 incident hemodialysis patients treated in 3 Canadian centers. MEASUREMENTS: We used mass spectrometry to measure plasma concentrations of the 25 elements at baseline, 6 months, 1 year, and 2 years following enrollment in the cohort. We focused on low concentrations of zinc, selenium, and manganese and excessive concentrations of lead, arsenic, and mercury; low and excessive concentrations of the other 19 trace elements were treated as exploratory analyses. Low and excessive concentrations were based on the 5th and 95th percentile plasma concentrations from healthy reference populations. RESULTS: At all 4 occasions, low zinc, selenium, and manganese concentrations were uncommon in study participants (≤5.1%, ≤1.8%, and ≤0.9% for zinc, selenium, and manganese, respectively) and a substantial proportion of participants had concentrations that exceeded the 95th percentile (≥65.2%, ≥74.2%, and ≥19.7%, respectively). Almost all participants had plasma lead concentrations above the 95th percentile at all time points. The proportion of participants with plasma arsenic concentrations exceeding the 95th percentile was relatively constant over time (9.1%-9.8%); the proportion with plasma mercury concentrations that exceeded the 95th percentile varied between 15.2% and 29.3%. Low arsenic, platinum, tungsten, and beryllium concentrations were common (>50%), as were excessive cobalt, manganese, zinc, vanadium, cadmium, selenium, barium, antimony, nickel, molybdenum, lead, and chromium concentrations. CONCLUSIONS: There was no evidence that low zinc, selenium, or manganese concentrations exist in most contemporary Canadian hemodialysis patients. Some patients have excessive plasma arsenic and mercury concentrations, and excessive lead concentrations were common. These findings require further investigation.


Assuntos
Falência Renal Crônica/sangue , Oligoelementos/sangue , Adolescente , Adulto , Idoso , Antimônio/sangue , Arsênio/sangue , Bário/sangue , Berílio/sangue , Cádmio/sangue , Cromo/sangue , Cobalto/sangue , Estudos de Coortes , Feminino , Humanos , Falência Renal Crônica/terapia , Chumbo/sangue , Masculino , Manganês/sangue , Espectrometria de Massas , Mercúrio/sangue , Pessoa de Meia-Idade , Molibdênio/sangue , Níquel/sangue , Platina/sangue , Estudos Prospectivos , Diálise Renal , Selênio/sangue , Tungstênio/sangue , Vanádio/sangue , Adulto Jovem , Zinco/sangue
2.
Transplantation ; 99(5): 985-90, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-25340607

RESUMO

BACKGROUND: Establishment of a national kidney paired donation (KPD) program represents a unique achievement in Canada's provincially organized health care system. METHODS: Key factors enabling program implementation included consultation with international experts, formation of a unique organization with a mandate to facilitate interprovincial collaboration, and the volunteer efforts of members of the Canadian transplant community to overcome a variety of logistical barriers. RESULTS: As of December 2013, the program had facilitated 240 transplantations including 10% with Calculated panel reactive antibody (cPRA) ≥97%. Unique features of the Canadian KPD program include participation of n = 55 nondirected donors, performance of only donor specific antibody negative transplants, the requirement for donor travel, and nonuse of bridge donors. CONCLUSION: The national KPD program has helped maintain the volume of living kidney donor transplants in Canada over the past 5 years and serves as a model of inter-provincial collaboration to improve the delivery of health care to Canadians.


Assuntos
Transplante de Rim , Doadores Vivos , Sistema ABO de Grupos Sanguíneos/imunologia , Incompatibilidade de Grupos Sanguíneos , Canadá , Teste de Histocompatibilidade , Humanos , Programas Nacionais de Saúde
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