Leg Ischaemia Management Collaboration (LIMb)
Single-centre prospective cohort study of patients presenting with severe limb ischaemia (SLI). The primary outcome measure will be 12 month major amputation rate. A historical cohort of patients identified retrospectively will be the comparitor group used to assess the impact of a newly-established rapid-access limb salvage clinic.
Primary aim:
- Determine the proportion of patients with SLI undergoing major lower limb amputation within 12 months of presentation.
Secondary aims:
- Assess clinically important short-, medium- and long-term outcomes in those undergoing and not undergoing amputation
- Prevalence and degree of frailty and cognitive impairment
- Pevalence and degree of cardiac disease (detected by stress MRI)
- Establish a biobank for future biomarker analysis
- Investigate the role of frailty and cognitive assessments, cardiac MRI and biomarkers in risk-stratification of patients with SLI
Visão geral do estudo
Status
Descrição detalhada
Severe limb ischaemia (SLI) is the end-stage of peripheral arterial occlusive disease (PAOD) whereby the viability of the limb is threatened due to the degree of arterial disease and subsequent ischaemia in the peripheral tissues. It is defined as ischaemic rest pain (or night pain) and/or ulceration or gangrene in the affected limb(s) for a minimum of two weeks attributed to confirmed PAOD. Treatment includes open surgical and endovascular revascularisation, with or without surgical debridement of affected tissues, amputation of toes and drainage of sepsis. In some patients revascularisation is not possible or fails resulting in the person requiring a major lower limb amputation.
Over 4000 major lower limb amputations per year were undertaken in England alone between 2003 and 2013 and a diabetes-related major lower limb amputation is performed every 30 seconds world-wide. As many as 25% of people with SLI will undergo a major lower limb amputation in the first year after presentation. Amputation negatively affects quality of life due to its negative impact on mobility, independence and ability to carry out activities of daily living.
This single-centre prospective cohort study will investigate the amputation rate at one year in patients presenting with SLI and compare this to a retrospectively identified historical cohort. This study will also investigate the prevelance and degree of frailty, cognitive impairment, and cardiac disease (detected by cardiac magnetic resonance imaging (MRI)), as well as establish a biobank for future biomarker analyses. The role of frailty and cognitive assessments, cardiac MRI and biomarker analysis in risk-stratifying patients with SLI will also be investigated.
Tipo de estudo
Inscrição (Antecipado)
Contactos e Locais
Contato de estudo
- Nome: Rob D Sayers, MD
- Número de telefone: +44 (0)116 252 3141
- E-mail: rs152@le.ac.uk
Estude backup de contato
- Nome: Tanya J Payne, BSc
- Número de telefone: +44 (0)116 258 3867
- E-mail: tjp28@le.ac.uk
Locais de estudo
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Leicestershire
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Leicester, Leicestershire, Reino Unido, LE3 9QP
- Recrutamento
- Glenfield Hospital Leicester
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Subinvestigador:
- Gerry P McCann, MD
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Contato:
- Tanya J Payne
- Número de telefone: +44 (0)116 358 3867
- E-mail: tjp28@le.ac.uk
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Investigador principal:
- Rob D Sayers, MD
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Subinvestigador:
- Matt J Bown, MD
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Subinvestigador:
- Thompson G Robinson, MD
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Subinvestigador:
- Victoria J Haunton, MD
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Subinvestigador:
- Sally J Singh, PhD
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Investigador principal:
- Robert SM Davies, MD
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Subinvestigador:
- Tanya J Payne, BSc
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Subinvestigador:
- Laura J Gray, PhD
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Subinvestigador:
- Harjeet S Rayt, MD
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Subinvestigador:
- Gregory S McMahon, MD
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Método de amostragem
População do estudo
Descrição
PRIMARY COHORT
Inclusion Criteria:
- All patients presenting to the Leicester Vascular Institute with SLI
Exclusion Criteria:
- SLI not caused by PAOD
- Patients undergoing intervention during their index presentation prior to recruitment
- Patients lacking capacity to consent with no accompanying next of kin, relative, partner or friend who can act as a personal consulted
- Patients who cannot read, write or understand English
- Any significant disease or disorder which may either put the patient at risk because of participation in the study, or may influence the results of the study or the patient's ability to participate in the study
FRAILTY & COGNITIVE ADDITIONAL ASSESSMENTS
Inclusion criteria:
- Patients recruited to the primary cohort in whom a decision has been made to undergo an intervention for SLI
- Patients aged ≥65 years
Exclusion criteria:
- Nil additional
CARDIAC MRI ADDITIONAL ASSESSMENTS
Inclusion criteria:
- Patients recruited to the primary cohort in whom a decision has been made to undergo an intervention
Exclusion criteria:
- Absolute contraindications to cardiac MRI (Pregnancy, Non-MR safe permanent pacemaker, implanted cardiac defibrillator, intra-auricular implant or intra-cranial clips, severe claustrophobia, unstable angina)
- Contraindication to gadolinium contrast agent (Known adverse reaction, chronic renal failure (eGFR <30mL/min/1.73m^2))
- Patients lacking capacity to consent for cardiac MRI
BIOMARKERS ADDITIONAL ASSESSMENTS
- Patients recruited to the primary cohort in whom a decision has been made to undergo an intervention
Exclusion criteria:
- Nil additional
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
Coortes e Intervenções
Grupo / Coorte |
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Primary cohort
Any patient presenting to the Leicester Vascular Institute with SLI during the 2 year recruitment period (minimum 420 patients).
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Frailty & cognitive additional assessments
Any patient recruited to the primary cohort aged ≥65 years and undergoing an intervention for SLI (minimum 150 patients, target 210 patients).
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Cardiac MRI additional assessments
Any patient recruited to the primary cohort, with capacity to consent and undergoing an intervention for SLI (minimum 100 patients).
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Biomarkers additional assessments
Any patient recruited to the primary cohort and undergoing an intervention for SLI (no target recruitment set).
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Historical cohort
Retrospectively identified cohort of patients presenting to the study site with SLI between 2013 -15 (target 420).
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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12 month amputation rate
Prazo: 12 months post recruitment
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Proportion of patients undergoing major lower limb amputation
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12 months post recruitment
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Amputation free survival
Prazo: ≥12 months post recruitment
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Composite outcome measure of death or amputation
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≥12 months post recruitment
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All-cause mortality
Prazo: ≥12 months
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Death from any cause
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≥12 months
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Quality of life
Prazo: 12 and 24 months post recruitment
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Quality of life as measured by the Vascular Quality of Life questionnaire (VascuQoL)
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12 and 24 months post recruitment
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Disability
Prazo: 12 and 24 months post recruitment
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Level of disability as measured by the Barthel Index - Score 0-20; higher score = greater degree of functional independence/lower level of disability |
12 and 24 months post recruitment
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Clinical Frailty Scale
Prazo: Baseline, 12 and 24 months
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Prevalence and degree of frailty as measured by the Clinical Frailty Scale (CFS)
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Baseline, 12 and 24 months
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Anxiety & Depression
Prazo: Baseline, 12 and 24 months
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Prevalence and degree of anxiety and depression as measured by the Hospital Anxiety and Depression Scale (HADS)
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Baseline, 12 and 24 months
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Outras medidas de resultado
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Cognitive impairment (Frailty & Cognitive additional assessments only)
Prazo: Baseline, 3 and 12 months
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Prevalence of cognitive impairment as detected by the Montreal Cognitive Assessment (MoCA)
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Baseline, 3 and 12 months
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Post-operative delirium (Frailty & Cognitive additional assessments only)
Prazo: 24 and 72 hours post intervention
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Incidence of post-operative delirium as detected by the Single Question in Delirium (SQiD) +/- 4 A's Test for delirium (4AT)
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24 and 72 hours post intervention
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Prevalence of coronary artery disease (Cardiac MR additional assessments only)
Prazo: Baseline
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Prevalence of coronary artery disease as detected by stress cardiac MRI
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Baseline
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Incidence of peri-operative myocardial infarction (Cardiac MR additional assessments only)
Prazo: 2-4 months post intervention
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Incidence of peri-operative myocardial infarction as detected by cardiac MRI
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2-4 months post intervention
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Edmonton Frail Scale (Frailty & Cognitive additional assessments only)
Prazo: Baseline, 3 and 12 months
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Prevalence and degree of frailty as measured by the Edmonton Frail Scale (EFS)
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Baseline, 3 and 12 months
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Cadeira de estudo: Rob D Sayers, MD, University of Leicester
Publicações e links úteis
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Antecipado)
Conclusão do estudo (Antecipado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- 0686
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