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1.
Pediatr Nephrol ; 27(9): 1557-64, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22552884

ABSTRACT

BACKGROUND: Uremic vasculopathy, including vascular calcification, increases the risk for cardiovascular disease and mortality in chronic kidney disease (CKD) patients. We have investigated the prevalence and factors associated with vasculopathy in children undergoing peritoneal dialysis (PD) or hemodialysis (HD) in a single center. METHODS: Common carotid intima media thickness (cIMT) and its relation with demographics, biochemical parameters and medication was analyzed in 60 patients (mean age 12.9 ± 3.4 years; 27 girls) treated with PD (n = 31) or HD (n = 29) for 34 ± 34 months. Patients were divided into two groups: normal cIMT and increased cIMT. RESULTS: Mean levels of calcium, phosphate and calcium/phosphate product were in the normal range, the but parathyroid hormone level, 729 ± 670 pg/mL, was higher than the National Kidney Foundation Kidney Disease Outcome Quality Iniative (K/DOQI) recommendations. Twenty-nine patients had increased cIMT, which was associated with time on dialysis of >2 years, hypercalcemia, higher daily dose of calcitriol and HD (vs. PD). In the multivariate analysis, accounting for time on dialysis, HD persisted as a risk for increased cIMT. CONCLUSIONS: The prevalence of increased cIMT in children on dialysis is similar to that reported in adults with CKD and increased with time on dialysis. HD was associated with increased cIMT, independently of time on dialysis; however, the results should be interpreted with caution due to the possible impact of confounding factors. These results underline the need to monitor and, if possible, prevent and treat increased cIMT in children on dialysis.


Subject(s)
Carotid Intima-Media Thickness , Peritoneal Dialysis/adverse effects , Renal Dialysis/adverse effects , Cardiovascular Diseases/epidemiology , Cardiovascular Diseases/etiology , Child , Child, Preschool , Cross-Sectional Studies , Female , Humans , Kidney Failure, Chronic/therapy , Male , Prevalence
2.
Rev. Soc. Esp. Enferm. Nefrol ; 14(4): 215-225, oct.-dic. 2011. tab
Article in Spanish | IBECS | ID: ibc-93839

ABSTRACT

Introducción: El cebado de las líneas de hemodiálisis (HD) se realiza de forma tradicional con heparina sódica y suero salino, lo que conlleva el riesgo hemorrágico que supone el paso de heparina a la sangre. Objetivo: Comparar el cebado del dializador de HD con o sin heparina sódica, en términos de coagulación, eficacia dialítica y eficacia económica. Material y métodos: Estudio prospectivo y randomizado de 3482 sesiones de 109 pacientes en HD (X 66,8±15 años, 40% mujeres, 44% diabéticos, 45% con catéter tunelizado de alto flujo, 50% FAVi nativa, 5% FAVi protésica). 1827 sesiones realizadas a cincuenta y nueve pacientes se incluyeron en el grupo control (cebado con suero fisiológico+heparina sódica) y 1455 de cincuenta pacientes en el grupo estudio (cebado con suero fisiológico). El periodo de seguimiento fue de 5 meses. Se analizaron variables relacionadas con la coagulación del circuito y la eficacia de la diálisis: Flujo de sangre (Qb) seleccionado y Qb efectivo, estado final del dializador, nº de cambios de dializador, nº de cambios de línea arterial, nº de cambios de línea venosa, Kt/hora medido por dialisancia iónica y heparinización del circuito. También se estudió la eficacia en términos económicos. Resultados: No existen diferencias significativas en los resultados relacionados con la coagulación y la eficacia de la diálisis obtenidos en ambos grupos, salvo la X de heparina de bajo peso molecular (2476±1089 Ui grupo estudio vs 2854±1414 Ui grupo control). El cebado sin heparina supone un ahorro de 0,5 e por sesión. Conclusiones: El cebado con suero fisiológico no influye en la dosis de HD, ni implica mayor riesgo de coagulación del sistema en comparación al cebado que añade heparina, evita el riesgo de paso de heparina a la circulación, disminuye la manipulación en los protocolos de conexión y reduce costes (AU)


Introduction: Haemodialysis (HD) lines are traditionally primed with sodium heparin and saline solution, which entails the haemorrhagic risk associated to the passing of heparin into the blood. Aim: To compare HD dialyser priming with and without sodium heparin, in terms of coagulation, dialytic efficacy, and economic efficacy. Material and Method: A randomized, prospective studio of 3482 sessions with 109 HD patients (X 66.8±15 years, 40% women, 44% diabetic, 45% with high-flow tunnelled catheter, 50% native IAF, 5% prosthetic IAF). 1827 sessions carried out with fifty-nine patients were included in the control group (primed with saline solution + sodium heparin) and 1455 sessions with patients in the study group (primed with saline solution). The monitoring period was 5 months. Variables related to the coagulation of the circuit and the efficacy of the dialysis were analysed: Selected blood flow (Qb) and effective Qb, final status of the dialyser, number of changes of dialyser, number of changes of the arterial line, number of changes of the venous, average Kt/hour measured by ionic dialysance and heparinization of the circuit. The efficacy in economic terms was also studied. Results: There are no significant differences in the results related to coagulation and efficacy of the dialysis obtained in both groups, except X of heparin with low molecular weight (2476±1089 IU in the study group compared to 2854±1414 IU in the control group). Priming without heparin represents a saving of 0.50 € per session. Conclusions: Priming with saline solution does not affect the HD dose, and does not entail a greater risk of coagulation of the system compared to a priming solution to which heparin has been added, avoids the risk of heparin passing into the bloodstream, reduces handling in the connection protocols and reduces costs (AU)


Subject(s)
Humans , Male , Female , Heparin/analysis , Hemodialysis Units, Hospital/organization & administration , Hemodialysis Solutions/metabolism , Hemodialysis Solutions/therapeutic use , Renal Dialysis/instrumentation , Blood Coagulation , Blood Coagulation/physiology , Prospective Studies , Clinical Protocols/standards , 28599
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