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10.1186/s12882-017-0607-5 http://scihub22266oqcxt.onion/10.1186/s12882-017-0607-5 C5463396!5463396!28592254     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       BMC+Nephrol 2017 ; 18 (ä): ä Nephropedia Template TP {{tp|p=28592254|t=2017. CKD QLD: establishment of a chronic kidney disease CKD registry in Queensland, Australia |pdf=|usr=}}{{28592254}} gab.com Text CKD QLD: establishment of a chronic kidney disease CKD registry in Queensland, Australia JO: BMC Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=28592254 #FOAvip Background: Chronic kidney disease [CKD] is recognised as a global public health problem. Until recently, the majority of information informing on CKD has been generated from renal registries reporting on patients with end-stage kidney disease [ESKD] and on renal replacement therapy [RRT]. There has been a paucity of information on pre-dialysis CKD cohorts, and many issues related to these poorly described populations are unresolved. To this end, international organizations have called for CKD surveillance systems across all countries. Description: In Australia, we have responded by developing the Chronic Kidney Disease in Queensland [CKD.QLD] with three main platforms consisting of CKD Registry, clinical trials and development of biobank. This registry which is the core component of CKD surveillance was conceptualized specifically for the pre-dialysis population in the public health system in Queensland, Australia. Recruitment started in May 2011, and to date the Registry has evolved as one of the largest CKD cohorts in the world with recruitment close to 7000 patients. The Registry has had many outcomes, including being the nidus for Australia?s first National Health and Medical Research Council [NHMRC] CKD Centre of Research Excellence [CKD.CRE]. Conclusions: The Registry, with its linkage to Queensland Health datasets, is reporting, and is expected to continue generating, significant information on multiple aspects of CKD, its trajectory, management and patient outcomes. Intent of the CKD.CRE is to facilitate an expanded Registry network that has representation from health services, both public and private, across Australia. Electronic supplementary material: The online version of this article (doi:10.1186/s12882-017-0607-5) contains supplementary material, which is available to authorized users. Twit Text FOAVip CKD QLD: establishment of a chronic kidney disease CKD registry in Queensland, Australia ????BMC Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=28592254 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28592254 #FOAvip English Wikipedia <ref>{{Cite pmid|28592254}}</ref> CKD QLD: establishment of a chronic kidney disease CKD registry in Queensland, Australia #MMPMID28592254 Venuthurupalli SK; Hoy WE; Healy HG; Cameron A; Fassett RG BMC Nephrol 2017[]; 18 (ä): ä PMID28592254show ga Background: Chronic kidney disease [CKD] is recognised as a global public health problem. Until recently, the majority of information informing on CKD has been generated from renal registries reporting on patients with end-stage kidney disease [ESKD] and on renal replacement therapy [RRT]. There has been a paucity of information on pre-dialysis CKD cohorts, and many issues related to these poorly described populations are unresolved. To this end, international organizations have called for CKD surveillance systems across all countries. Description: In Australia, we have responded by developing the Chronic Kidney Disease in Queensland [CKD.QLD] with three main platforms consisting of CKD Registry, clinical trials and development of biobank. This registry which is the core component of CKD surveillance was conceptualized specifically for the pre-dialysis population in the public health system in Queensland, Australia. Recruitment started in May 2011, and to date the Registry has evolved as one of the largest CKD cohorts in the world with recruitment close to 7000 patients. The Registry has had many outcomes, including being the nidus for Australia?s first National Health and Medical Research Council [NHMRC] CKD Centre of Research Excellence [CKD.CRE]. Conclusions: The Registry, with its linkage to Queensland Health datasets, is reporting, and is expected to continue generating, significant information on multiple aspects of CKD, its trajectory, management and patient outcomes. Intent of the CKD.CRE is to facilitate an expanded Registry network that has representation from health services, both public and private, across Australia. Electronic supplementary material: The online version of this article (doi:10.1186/s12882-017-0607-5) contains supplementary material, which is available to authorized users. äCKD QLD: establishment of a chronic kidney disease CKD registry in Q(epmc).pdf DeepDyve Pubget Overpricing