Editor's Choice - Recommendations for Registry Data Collection for Revascularisations of Acute Limb Ischaemia
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Editor's Choice - Recommendations for Registry Data Collection for Revascularisations of Acute Limb Ischaemia : A Delphi Consensus from the International Consortium of Vascular Registries. / Behrendt, Christian-Alexander; Björck, Martin; Schwaneberg, Thea; Debus, Eike S; Cronenwett, Jack; Sigvant, Birgitta; Acute Limb Ischaemia Collaborators.
In: EUR J VASC ENDOVASC, Vol. 57, No. 6, 06.2019, p. 816-821.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Editor's Choice - Recommendations for Registry Data Collection for Revascularisations of Acute Limb Ischaemia
T2 - A Delphi Consensus from the International Consortium of Vascular Registries
AU - Behrendt, Christian-Alexander
AU - Björck, Martin
AU - Schwaneberg, Thea
AU - Debus, Eike S
AU - Cronenwett, Jack
AU - Sigvant, Birgitta
AU - Acute Limb Ischaemia Collaborators
N1 - Copyright © 2019 European Society for Vascular Surgery. All rights reserved.
PY - 2019/6
Y1 - 2019/6
N2 - OBJECTIVE: To develop a minimum core data set for evaluation of acute limb ischaemia (ALI) revascularisation treatment and outcomes that would enable collaboration among international registries.METHODS: A modified Delphi approach was used to achieve consensus among international multidisciplinary vascular specialists and registry members of the International Consortium of Vascular Registries (ICVR). Variables identified in the literature or suggested by the expert panel, and variables, including definitions, currently used in 15 countries in the ICVR, were assessed to define both a minimum core and an optimum data set to register ALI treatment. Clinical relevance and practicability were both assessed, and consensus was defined as ≥ 80% agreement among participants.RESULTS: Of 40 invited experts, 37 completed a preliminary survey and 31 completed the two subsequent Delphi rounds via internet exchange and face to face discussions. In total, 117 different items were generated from the various registry data forms, an extensive review of the literature, and additional suggestions from the experts, for potential inclusion in the data set. Ultimately, 35 items were recommended for inclusion in the minimum core data set, including 23 core items important for all registries, and an additional 12 more specific items for registries capable of capturing more detail. These 35 items supplement previous data elements recommended for registering chronic peripheral arterial occlusive disease treatment.CONCLUSION: A modified Delphi study allowed 37 international vascular registry experts to achieve a consensus recommendation for a minimum core and an optimum data set for registries covering patients who undergo ALI revascularisation. Continued global harmonisation of registry infrastructure and definition of items allows international comparisons and global quality improvement. Furthermore, it can help to define and monitor standards of care and enable international research collaboration.
AB - OBJECTIVE: To develop a minimum core data set for evaluation of acute limb ischaemia (ALI) revascularisation treatment and outcomes that would enable collaboration among international registries.METHODS: A modified Delphi approach was used to achieve consensus among international multidisciplinary vascular specialists and registry members of the International Consortium of Vascular Registries (ICVR). Variables identified in the literature or suggested by the expert panel, and variables, including definitions, currently used in 15 countries in the ICVR, were assessed to define both a minimum core and an optimum data set to register ALI treatment. Clinical relevance and practicability were both assessed, and consensus was defined as ≥ 80% agreement among participants.RESULTS: Of 40 invited experts, 37 completed a preliminary survey and 31 completed the two subsequent Delphi rounds via internet exchange and face to face discussions. In total, 117 different items were generated from the various registry data forms, an extensive review of the literature, and additional suggestions from the experts, for potential inclusion in the data set. Ultimately, 35 items were recommended for inclusion in the minimum core data set, including 23 core items important for all registries, and an additional 12 more specific items for registries capable of capturing more detail. These 35 items supplement previous data elements recommended for registering chronic peripheral arterial occlusive disease treatment.CONCLUSION: A modified Delphi study allowed 37 international vascular registry experts to achieve a consensus recommendation for a minimum core and an optimum data set for registries covering patients who undergo ALI revascularisation. Continued global harmonisation of registry infrastructure and definition of items allows international comparisons and global quality improvement. Furthermore, it can help to define and monitor standards of care and enable international research collaboration.
KW - Acute Disease
KW - Consensus
KW - Data Collection/standards
KW - Delphi Technique
KW - Humans
KW - Ischemia/diagnosis
KW - Registries/standards
KW - Risk Assessment
KW - Risk Factors
KW - Treatment Outcome
KW - Vascular Surgical Procedures/adverse effects
U2 - 10.1016/j.ejvs.2019.02.023
DO - 10.1016/j.ejvs.2019.02.023
M3 - SCORING: Journal article
C2 - 31128987
VL - 57
SP - 816
EP - 821
JO - EUR J VASC ENDOVASC
JF - EUR J VASC ENDOVASC
SN - 1078-5884
IS - 6
ER -
