(C) 2013 Elsevier Ireland Ltd All rights reserved “
“Object

(C) 2013 Elsevier Ireland Ltd. All rights reserved.”
“Objective: The peritoneal equilibration test (PET) using 3.86% glucose solution is preceded by a long dwell with 3.86% glucose solution. A point of concern in patients treated with automated

peritoneal dialysis (APD) is the influence of the preceding short nightly LGX818 MAPK inhibitor dwells on the results of a standardized PET. The aim of the study was to compare net ultrafiltration, small solute transport, sodium sieving, and solute transport type between a PET preceded by a long night dwell and one preceded by short (APD) dwells.

Patients and Methods: 13 stable APD patients (mean age 60 +/- 15 years; mean duration of peritoneal dialysis 31 +/- 15 months) underwent 2 PETs: 1 preceded by short nightly dwells (PET A) and 1 preceded by a long night dwell (PET B).

Results: Both PETs were performed within a mean period of 8 (range 5-11) days. Mean total ultrafiltration of PET A was 626 +/- 218 mL and PET B was 644 +/- 223 mL (NS). The 4-hour results of both tests for dialysate-to-plasma (D/P) ratios of creatinine and urea, D(t)/D(0) ratios of glucose, and the dip in D/P sodium (sodium sieving) were similar. Classification of transport categories was identical for 10 of 13 patients.

Conclusion: In APD, the preceding

dwell time of a 3.86% glucose PET does not influence fluid transport, solute transport, or transport type.”
“Objective: The high frequency of risk factors detected within the newborn population

increases the total number of children that should receive regular follow-ups. However, in some Entrectinib purchase circumstances, this could be beyond the capacity of the health system. Therefore, careful interpretation and selection of risk factors, and in particular of those factors not strictly defined, should be carried out during screening. The aim of the study was to analyse the risk factor profile of children covered by the national universal neonatal hearing screening program and to correlate it with hearing loss incidence.

Patients and methods: The analysis of records in the program database collected from 472 neonatal and well-baby units over a period of 10 years (2002-2012), focused on children with at least one risk factor. The analysis was subdivided into distribution of risk factors as well as to risk factors and hearing loss correlation.

Results: In the studied cohort of n = 137,432 children (4% BAY 73-4506 molecular weight of the total number of screened children) single risk factors were most frequently detected, accounting for 71% of records. The association of two or more risk factors appeared in 659 configurations (29%), with a mean of 3.1 coexisting risk factors and a maximum of 9. Hearing loss was dependent on the number of risk factors in a child, but reached its maximum with the association of 6 factors.

Conclusions: The detection of postnatal hearing loss should be continued in order to increase our understanding of hearing incidence and the role of environmental factors.

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