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Serum phosphate optimal timing and range associated with patients survival in haemodialysis: The COSMOS study
dc.contributor.author | Fernández-Martín J.L. | |
dc.contributor.author | Dusso A. | |
dc.contributor.author | Martínez-Camblor P. | |
dc.contributor.author | Dionisi M.P. | |
dc.contributor.author | Floege J. | |
dc.contributor.author | Ketteler M. | |
dc.contributor.author | London G. | |
dc.contributor.author | Locatelli F. | |
dc.contributor.author | Górriz J.L. | |
dc.contributor.author | Rutkowski B. | |
dc.contributor.author | Bos W.-J. | |
dc.contributor.author | Tielemans C. | |
dc.contributor.author | Martin P.-Y. | |
dc.contributor.author | Wüthrich R.P. | |
dc.contributor.author | Pavlovic D. | |
dc.contributor.author | Benedik M. | |
dc.contributor.author | Rodríguez-Puyol D. | |
dc.contributor.author | Carrero J.J. | |
dc.contributor.author | Zoccali C. | |
dc.contributor.author | Cannata-Andía J.B. | |
dc.contributor.author | Covic A. | |
dc.contributor.author | Ferreira A. | |
dc.contributor.author | Goldsmith D. | |
dc.contributor.author | Kramar R. | |
dc.contributor.author | Memmos D. | |
dc.contributor.author | Nagy J. | |
dc.contributor.author | Teplan V. | |
dc.contributor.author | Verbeelen D. | |
dc.contributor.author | Motellón J.L. | |
dc.contributor.author | Turner M. | |
dc.contributor.author | Chaussy J. | |
dc.contributor.author | Molemans B. | |
dc.contributor.author | Zani W. | |
dc.contributor.author | Rosser D. | |
dc.contributor.author | Dehmel B. | |
dc.contributor.author | Fouqueray B. | |
dc.contributor.author | Bradbury B. | |
dc.contributor.author | Acquavella J. | |
dc.contributor.author | Hollowell J. | |
dc.contributor.author | Carter D. | |
dc.contributor.author | Holland P. | |
dc.contributor.author | Baños A. | |
dc.contributor.author | Mattin C. | |
dc.contributor.author | Critchlow C. | |
dc.contributor.author | Kim J. | |
dc.contributor.author | Lewis C. | |
dc.contributor.author | Panayi A. | |
dc.contributor.author | Hemetsberger M. | |
dc.contributor.author | Croft S. | |
dc.contributor.author | Jaeger P. | |
dc.contributor.author | Muehlebach P. | |
dc.contributor.author | Blackburn J. | |
dc.contributor.author | Zumsteg E. | |
dc.contributor.author | Rodríguez S. | |
dc.contributor.author | Pérez A. | |
dc.contributor.author | Faner P. | |
dc.contributor.author | Izco I. | |
dc.contributor.author | Traseira S. | |
dc.contributor.author | Castro C. | |
dc.contributor.author | Moreno J. | |
dc.contributor.author | Calle D. | |
dc.contributor.author | Pieraccini F. | |
dc.date.accessioned | 2020-09-02T22:17:29Z | |
dc.date.available | 2020-09-02T22:17:29Z | |
dc.date.issued | 2019 | |
dc.identifier | 10.1093/ndt/gfy093 | |
dc.identifier.citation | 34, 4, 673-681 | |
dc.identifier.issn | 09310509 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12728/4454 | |
dc.description | Background. Serum phosphate is a key parameter in the management of chronic kidney disease-mineral and bone disorder (CKD-MBD). The timing of phosphate measurement is not standardized in the current guidelines. Since the optimal range of these biomarkers may vary depending on the duration of the interdialytic interval, in this analysis of the Current management of secondary hyperparathyroidism: a multicentre observational study (COSMOS), we assessed the influence of a 2- (midweek) or 3-day (post-weekend) dialysis interval for blood withdrawal on serum levels of CKD-MBD biomarkers and their association with mortality risk. Methods. The COSMOS cohort (6797 patients, CKD Stage 5D) was divided into two groups depending upon midweek or post-weekend blood collection. Univariate and multivariate Cox's models adjusted hazard ratios (HRs) by demographics and comorbidities, treatments and biochemical parameters from a patient/centre database collected at baseline and every 6 months for 3 years. Results. There were no differences in serum calcium or parathyroid hormone levels between midweek and post-weekend patients. However, in post-weekend patients, the mean serum phosphate levels were higher compared with midweek patients (5.5 ± 1.4 versus 5.2 ± 1.4 mg/dL, P < 0.001). Also, the range of serum phosphate with the lowest mortality risk [HR ≤ 1.1; midweek: 3.5-4.9 mg/dL (95% confidence interval, CI: 2.9-5.2 mg/dL); post-weekend: 3.8-5.7 mg/dL (95% CI: 3.0-6.4 mg/dL)] showed significant differences in the upper limit (P = 0.021). Conclusion. Midweek and post-weekend serum phosphate levels and their target ranges associated with the lowest mortality risk differ. Thus, clinical guidelines should consider the timing of blood withdrawal when recommending optimal target ranges for serum phosphate and therapeutic strategies for phosphate control. © 2018 The Author(s). | |
dc.language.iso | en | |
dc.publisher | Oxford University Press | |
dc.subject | calcaemia | |
dc.subject | chronic haemodialysis | |
dc.subject | epidemiology | |
dc.subject | hyperparathyroidism | |
dc.subject | phosphataemia | |
dc.subject | albumin | |
dc.subject | biological marker | |
dc.subject | calcium | |
dc.subject | hemoglobin | |
dc.subject | parathyroid hormone | |
dc.subject | phosphate | |
dc.subject | biological marker | |
dc.subject | calcium | |
dc.subject | parathyroid hormone | |
dc.subject | phosphate | |
dc.subject | adult | |
dc.subject | albumin blood level | |
dc.subject | all cause mortality | |
dc.subject | Article | |
dc.subject | blood sampling | |
dc.subject | body mass | |
dc.subject | calcium blood level | |
dc.subject | chronic kidney disease-mineral and bone disorder | |
dc.subject | clinical assessment | |
dc.subject | cohort analysis | |
dc.subject | comorbidity | |
dc.subject | female | |
dc.subject | hemodialysis | |
dc.subject | hemoglobin blood level | |
dc.subject | human | |
dc.subject | major clinical study | |
dc.subject | male | |
dc.subject | middle aged | |
dc.subject | mortality risk | |
dc.subject | multicenter study | |
dc.subject | observational study | |
dc.subject | parathyroid hormone blood level | |
dc.subject | phosphate blood level | |
dc.subject | priority journal | |
dc.subject | prospective study | |
dc.subject | blood | |
dc.subject | chronic kidney disease-mineral and bone disorder | |
dc.subject | clinical trial | |
dc.subject | hemodialysis | |
dc.subject | mortality | |
dc.subject | prognosis | |
dc.subject | randomization | |
dc.subject | secondary hyperparathyroidism | |
dc.subject | survival rate | |
dc.subject | Biomarkers | |
dc.subject | Calcium | |
dc.subject | Chronic Kidney Disease-Mineral and Bone Disorder | |
dc.subject | Female | |
dc.subject | Humans | |
dc.subject | Hyperparathyroidism, Secondary | |
dc.subject | Male | |
dc.subject | Middle Aged | |
dc.subject | Parathyroid Hormone | |
dc.subject | Phosphates | |
dc.subject | Prognosis | |
dc.subject | Prospective Studies | |
dc.subject | Random Allocation | |
dc.subject | Renal Dialysis | |
dc.subject | Survival Rate | |
dc.title | Serum phosphate optimal timing and range associated with patients survival in haemodialysis: The COSMOS study | |
dc.type | Article |