International quotidian dialysis registry: Annual report 2010
Identifieur interne : 000228 ( Istex/Curation ); précédent : 000227; suivant : 000229International quotidian dialysis registry: Annual report 2010
Auteurs : Robert M. Lindsay [Canada] ; Rita S. Suri [Canada] ; Louise M. Moist [Canada] ; Amit X. Garg [Canada] ; Meaghan Cuerden [Canada] ; Sarah Langford [Canada] ; Raymond Hakim [États-Unis] ; Norma J. Ofsthun [États-Unis] ; Stephen P. Mcdonald [Australie] ; Carmel Hawley [Australie] ; Ferqus J. Caskey [Royaume-Uni] ; Cecile Couchoud [France] ; Christian Awaraji [Canada] ; Gihad E. Nesrallah [Canada]Source :
- Hemodialysis International [ 1492-7535 ] ; 2011-01.
Descripteurs français
- Wicri :
- topic : Rapport d'activité, Réseau d'information.
English descriptors
- KwdEn :
- Adeera levin, Advisory board, Annual report, Anzdata registry, Baseline crfs, Canadian iqdr data, Centre, Clinical events, Clinical trials, Cohort studies, Collaborative studies, Commercial databases, Conventional hemodialysis, Corporate research, Current research agenda, Data sources, Dialysis prescription, Frequent hemodialysis network, Governance model, Hemodialysis, Information network, Initial patient registration, Intermediate outcomes, International quotidian dialysis registry, International society, Iqdr, Kidney centers, Laboratory parameters, Large cohort studies, Lindsay, London health sciences centre, National institutes, National registries, Nephrol dial transplant, Nephrology meeting, Nesrallah, Nocturnal, Nocturnal hemodialysis, Ontario, Operational group, Outcome areas, Peritoneal dialysis, Physical data, Physical parameters, Pierratos, Prevalent patients, Primary data, Primary data collection methods, Primary data sources, Princess alexandra hospital, Quotidian, Quotidian dialysis, Quotidian hemodialysis, Randomized, Randomized trials, Regimen, Registry, Renal, Renal registry, Research agenda, Sdhd, Semiannual basis, Study design, Suri, Surrogate outcomes, Technique survival, Transplant registry, Vascular access, Vascular access outcomes, Ventricular mass, Western ontario, Zealand dialysis.
- Teeft :
- Adeera levin, Advisory board, Annual report, Anzdata registry, Baseline crfs, Canadian iqdr data, Centre, Clinical events, Clinical trials, Cohort studies, Collaborative studies, Commercial databases, Conventional hemodialysis, Corporate research, Current research agenda, Data sources, Dialysis prescription, Frequent hemodialysis network, Governance model, Hemodialysis, Information network, Initial patient registration, Intermediate outcomes, International quotidian dialysis registry, International society, Iqdr, Kidney centers, Laboratory parameters, Large cohort studies, Lindsay, London health sciences centre, National institutes, National registries, Nephrol dial transplant, Nephrology meeting, Nesrallah, Nocturnal, Nocturnal hemodialysis, Ontario, Operational group, Outcome areas, Peritoneal dialysis, Physical data, Physical parameters, Pierratos, Prevalent patients, Primary data, Primary data collection methods, Primary data sources, Princess alexandra hospital, Quotidian, Quotidian dialysis, Quotidian hemodialysis, Randomized, Randomized trials, Regimen, Registry, Renal, Renal registry, Research agenda, Sdhd, Semiannual basis, Study design, Suri, Surrogate outcomes, Technique survival, Transplant registry, Vascular access, Vascular access outcomes, Ventricular mass, Western ontario, Zealand dialysis.
Abstract
The International Quotidian Dialysis Registry (IQDR) is a global initiative designed to study practices and outcomes associated with the use of hemodialysis (HD) regimens of increased frequency and/or duration. The IQDR grew out of the initiative that lead to the randomized prospective studies of nocturnal HD and short hours daily dialysis vs. conventional thrice weekly HD that are conducted by the Frequent Hemodialysis Network sponsored by the National Institutes of Health. These 2 separate studies are drawing to a close and the first results are expected to be reported later this year. These studies use surrogate outcomes for their primary endpoints as they are not powered to look at outcomes of mortality and hospitalization. The IQDR attempts to aggregate long‐term follow‐up data from centers utilizing alternative HD regimens worldwide and will have adequate statistical power to examine those important outcomes. To date, the IQDR has enrolled patients from Canada, the United States, Australia, New Zealand, and France and has linked with commercial databases and national registries. This sixth annual report of the IQDR describes: (1) An update on the governance structure; (2) The recommendations made at the first general meetings of the IQDR Scientific Committee and Advisory Board; (3) The status of those recommendations; (4) A summary of current data sources and participating registries; (5) The status of recruitment to date; (6) The creation of a specific Canadian IQDR data set and; (7) The current research agenda.
Url:
DOI: 10.1111/j.1542-4758.2010.00521.x
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ISTEX:0B9D34642851F08B4B5741E9A9B90BEAAEE79ADDLe document en format XML
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adeera levin</term>
<term>Advisory board</term>
<term>Annual report</term>
<term>Anzdata registry</term>
<term>Baseline crfs</term>
<term>Canadian iqdr data</term>
<term>Centre</term>
<term>Clinical events</term>
<term>Clinical trials</term>
<term>Cohort studies</term>
<term>Collaborative studies</term>
<term>Commercial databases</term>
<term>Conventional hemodialysis</term>
<term>Corporate research</term>
<term>Current research agenda</term>
<term>Data sources</term>
<term>Dialysis prescription</term>
<term>Frequent hemodialysis network</term>
<term>Governance model</term>
<term>Hemodialysis</term>
<term>Information network</term>
<term>Initial patient registration</term>
<term>Intermediate outcomes</term>
<term>International quotidian dialysis registry</term>
<term>International society</term>
<term>Iqdr</term>
<term>Kidney centers</term>
<term>Laboratory parameters</term>
<term>Large cohort studies</term>
<term>Lindsay</term>
<term>London health sciences centre</term>
<term>National institutes</term>
<term>National registries</term>
<term>Nephrol dial transplant</term>
<term>Nephrology meeting</term>
<term>Nesrallah</term>
<term>Nocturnal</term>
<term>Nocturnal hemodialysis</term>
<term>Ontario</term>
<term>Operational group</term>
<term>Outcome areas</term>
<term>Peritoneal dialysis</term>
<term>Physical data</term>
<term>Physical parameters</term>
<term>Pierratos</term>
<term>Prevalent patients</term>
<term>Primary data</term>
<term>Primary data collection methods</term>
<term>Primary data sources</term>
<term>Princess alexandra hospital</term>
<term>Quotidian</term>
<term>Quotidian dialysis</term>
<term>Quotidian hemodialysis</term>
<term>Randomized</term>
<term>Randomized trials</term>
<term>Regimen</term>
<term>Registry</term>
<term>Renal</term>
<term>Renal registry</term>
<term>Research agenda</term>
<term>Sdhd</term>
<term>Semiannual basis</term>
<term>Study design</term>
<term>Suri</term>
<term>Surrogate outcomes</term>
<term>Technique survival</term>
<term>Transplant registry</term>
<term>Vascular access</term>
<term>Vascular access outcomes</term>
<term>Ventricular mass</term>
<term>Western ontario</term>
<term>Zealand dialysis</term>
</keywords>
<keywords scheme="Teeft" xml:lang="en"><term>Adeera levin</term>
<term>Advisory board</term>
<term>Annual report</term>
<term>Anzdata registry</term>
<term>Baseline crfs</term>
<term>Canadian iqdr data</term>
<term>Centre</term>
<term>Clinical events</term>
<term>Clinical trials</term>
<term>Cohort studies</term>
<term>Collaborative studies</term>
<term>Commercial databases</term>
<term>Conventional hemodialysis</term>
<term>Corporate research</term>
<term>Current research agenda</term>
<term>Data sources</term>
<term>Dialysis prescription</term>
<term>Frequent hemodialysis network</term>
<term>Governance model</term>
<term>Hemodialysis</term>
<term>Information network</term>
<term>Initial patient registration</term>
<term>Intermediate outcomes</term>
<term>International quotidian dialysis registry</term>
<term>International society</term>
<term>Iqdr</term>
<term>Kidney centers</term>
<term>Laboratory parameters</term>
<term>Large cohort studies</term>
<term>Lindsay</term>
<term>London health sciences centre</term>
<term>National institutes</term>
<term>National registries</term>
<term>Nephrol dial transplant</term>
<term>Nephrology meeting</term>
<term>Nesrallah</term>
<term>Nocturnal</term>
<term>Nocturnal hemodialysis</term>
<term>Ontario</term>
<term>Operational group</term>
<term>Outcome areas</term>
<term>Peritoneal dialysis</term>
<term>Physical data</term>
<term>Physical parameters</term>
<term>Pierratos</term>
<term>Prevalent patients</term>
<term>Primary data</term>
<term>Primary data collection methods</term>
<term>Primary data sources</term>
<term>Princess alexandra hospital</term>
<term>Quotidian</term>
<term>Quotidian dialysis</term>
<term>Quotidian hemodialysis</term>
<term>Randomized</term>
<term>Randomized trials</term>
<term>Regimen</term>
<term>Registry</term>
<term>Renal</term>
<term>Renal registry</term>
<term>Research agenda</term>
<term>Sdhd</term>
<term>Semiannual basis</term>
<term>Study design</term>
<term>Suri</term>
<term>Surrogate outcomes</term>
<term>Technique survival</term>
<term>Transplant registry</term>
<term>Vascular access</term>
<term>Vascular access outcomes</term>
<term>Ventricular mass</term>
<term>Western ontario</term>
<term>Zealand dialysis</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Rapport d'activité</term>
<term>Réseau d'information</term>
</keywords>
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<front><div type="abstract" xml:lang="en">The International Quotidian Dialysis Registry (IQDR) is a global initiative designed to study practices and outcomes associated with the use of hemodialysis (HD) regimens of increased frequency and/or duration. The IQDR grew out of the initiative that lead to the randomized prospective studies of nocturnal HD and short hours daily dialysis vs. conventional thrice weekly HD that are conducted by the Frequent Hemodialysis Network sponsored by the National Institutes of Health. These 2 separate studies are drawing to a close and the first results are expected to be reported later this year. These studies use surrogate outcomes for their primary endpoints as they are not powered to look at outcomes of mortality and hospitalization. The IQDR attempts to aggregate long‐term follow‐up data from centers utilizing alternative HD regimens worldwide and will have adequate statistical power to examine those important outcomes. To date, the IQDR has enrolled patients from Canada, the United States, Australia, New Zealand, and France and has linked with commercial databases and national registries. This sixth annual report of the IQDR describes: (1) An update on the governance structure; (2) The recommendations made at the first general meetings of the IQDR Scientific Committee and Advisory Board; (3) The status of those recommendations; (4) A summary of current data sources and participating registries; (5) The status of recruitment to date; (6) The creation of a specific Canadian IQDR data set and; (7) The current research agenda.</div>
</front>
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