“Objective Transcutaneous

bilirubin


“Objective. Transcutaneous

bilirubin LDK378 order (TcB) has the potential to reduce scrum bilirubin sampling. During a recent survey on the use of TcB in postnatal units in the Republic of Ireland, we identified that only 58% of the 19 units were using TcB and that only two devices were in use, the BiliChek (R) and JM 103 (R). We aimed to evaluate and compare these two devices in a regional postnatal unit.

Methods. To evaluate and compare the accuracy of the BiliChek (R) and JM 103, we studied simultaneous TcB and total serum bilirubin (TSB) measurements from a population of jaundiced term and near term infants. We evaluated each device with regard to correlation with TSB and potential to safely reduce scrum bilirubin testing.

Results. Both TcB devices strongly correlated with TSB (r=0.88 for BiliChek (R) and r=0.70 for JM 103 (R)). YM155 The BiliChek (R) and JM 103 (R) were accurate up to cut-off values of 200 mu mol/L and 180 mu

mol/L, respectively. Using Bhutani’s nomogram, 100% sensitivity was achieved using the 75th percentile for BiliChek (R) and the 40th percentile for JM 103 (R).

Conclusion. Both TcB devices correlated closely with moderately increased TSB levels and are suitable screening tools to identify jaundiced infants that require a scrum bilirubin, with upper limit cut-off values. Both devices reduced the need for TSB levels. We found the BiliChek (R) slightly more accurate than the JM 103 (R) for our study population. TcB however, BI-D1870 research buy is not in widespread use.”
“This systematic review considers the evidence available

for a relationship between periodontal disease and rheumatoid arthritis. MEDLINE/PubMed, CINAHL, DOSS, Embase, Scopus, Web of Knowledge, MedNar, and ProQuest Theses and Dissertations were searched from the inception of the database until June 2012 for any quantitative studies that examined the association between periodontal disease and rheumatoid arthritis. Nineteen studies met our inclusion criteria. Good evidence was found to support an association between these conditions with regard to tooth loss, clinical attachment levels, and erythrocyte sedimentation rates. Moderate evidence was noted for C-reactive protein and interleukin-1 beta. Some evidence for a positive outcome of periodontal treatment on the clinical features of rheumatoid arthritis was noted. These results provide moderate evidence based on biochemical markers and stronger evidence with regard to clinical parameters that common risk factors or common pathologic processes may be responsible for an association between rheumatoid arthritis and periodontal disease. Further studies are required to fully explore both the biochemical processes and clinical relationships between these 2 chronic inflammatory conditions.

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