Femoral nerve block Intervention in Neck of Femur fracture (FINOF): study protocol for a randomized controlled trial

被引:12
|
作者
Sahota, Opinder [1 ]
Rowlands, Martin [2 ]
Bradley, Jim [3 ]
de Walt, Gerrie Van [3 ]
Bedforth, Nigel [3 ]
Armstrong, Sarah [4 ]
Moppett, Iain [2 ]
机构
[1] Nottingham Univ Hosp NHS Trust, Dept Healthcare Older People, Nottingham NG7 2UH, England
[2] Univ Nottingham, Queens Med Ctr, Div Clin Neurosci, Anaesthesia & Crit Care Res Grp, Nottingham NG7 2RD, England
[3] Nottingham Univ Hosp NHS Trust, Nottingham NG7 2UH, England
[4] Univ Nottingham, Fac Med & Hlth Sci, NIHR Res Design Serv East Midlands, Queens Med Ctr, Nottingham NG7 2UH, England
来源
TRIALS | 2014年 / 15卷
基金
美国国家卫生研究院;
关键词
Elderly; Hip fracture; Hip surgery; Analgesia; Femoral nerve block; Femoral nerve catheter; Nerve block; ILIACA COMPARTMENT BLOCK; CONSENSUS RECOMMENDATIONS; HIP-FRACTURES; ANALGESIA; PAIN; SCORE; MORTALITY; REPAIR;
D O I
10.1186/1745-6215-15-189
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Hip fractures are very painful leading to lengthy hospital stays. Conventional methods of treating pain are limited. Non-steroidal anti-inflammatories are relatively contraindicated and opioids have significant side effects. Regional anaesthesia holds promise but results from these techniques are inconsistent. Trials to date have been inconclusive with regard to which blocks to use and for how long. Interpatient variability remains a problem. Methods/Design: This is a single centre study conducted at Queen's Medical Centre, Nottingham; a large regional trauma centre in England. It is a pragmatic, parallel arm, randomized controlled trial. Sample size will be 150 participants (75 in each group). Randomization will be web-based, using computer generated concealed tables (service provided by Nottingham University Clinical Trials Unit). There is no blinding. Intervention will be a femoral nerve block (0.5 mls/kg 0.25% levo-bupivacaine) followed by ropivacaine (0.2% 5 ml/hr(-1)) infused via a femoral nerve catheter until 48 hours post-surgery. The control group will receive standard care. Participants will be aged over 70 years, cognitively intact (abbreviated mental score of seven or more), able to provide informed consent, and admitted directly through the Emergency Department from their place of residence. Primary outcomes will be cumulative ambulation score (from day 1 to 3 postoperatively) and cumulative dynamic pain scores (day 1 to 3 postoperatively). Secondary outcomes will be cumulative dynamic pain score preoperatively, cumulative side effects, cumulative calorific and protein intake, EUROQOL EQ-5D score, length of stay, and rehabilitation outcome (measured by mobility score). Discussion: Many studies have shown the effectiveness of regional blockade in neck of femur fractures, but the techniques used have varied. This study aims to identify whether early and continuous femoral nerve block can be effective in relieving pain and enhancing mobilization. Trial registration.
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页数:6
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