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Peripheral Nerve Blocks in Elderly Patients With Hip Fracture

Not Applicable
Conditions
Hip Fracture
Registration Number
NCT02635763
Lead Sponsor
Shanghai Jiao Tong University Affiliated Sixth People's Hospital
Brief Summary

As the population ages, the frequency of surgery is increasing proportionally, bringing with it the challenge of managing older patients with frequent comorbid diseases and an increased risk of complications. Poor postoperative quality of recovery may result in patient and family suffering, a prolonged hospital stay, and a greater demand on health care resources.The purpose of this study was to evaluate the ultrasound guided percutaneous femoral nerve+lateral cutaneous nerve versus lumbar plexus+sacral plexus nerve block composite laryngeal mask anesthesia in elderly hip fracture surgery, the application of assessing their impact on the postoperative recovery quality.

Detailed Description

In this study, patients who were more than 65 years old with hip fracture were randomized to peripheral nerve blocks 1(PNBs1)- femoral nerve+lateral cutaneous nerve-with laryngeal mask anesthesia, or peripheral nerve blocks 2(PNBs2) - lumbar plexus and sciatic - with laryngeal mask anesthesia. Blocks were performed using ultrasound and 0.5% ropivacaine. All patients received postoperative multimodal analgesia. Postoperative recovery was assessed at 15 minutes, 40 minutes,- 1 day, 3 days, and 7 days after surgery, with the Postoperative Quality of Recovery Scale, in physiological, nociceptive, emotive, modified activities of daily living, modified cognitive, and overall patient perspective domains.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
60
Inclusion Criteria
  1. ASA grade I ~ III level;
  2. The BMI <30;
  3. The Mini - getting the state examination MMSE > 23;
  4. The operation type:open reduction and internal fixation or bipolar head replace.
Exclusion Criteria
  1. Serious systemic diseases such as respiratory dysfunction, cardiac insufficiency, and renal insufficiency;
  2. Has a history of cognitive function disorder or mental illness;
  3. Has a history of cerebral infarction and leave sequela;
  4. The blood coagulation dysfunction;
  5. The hearing or visual impairment;
  6. Unable to complete assessment;
  7. Operation time more than 90 minutes;
  8. The bleeding is greater than 1000 ml.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
postoperative quality of recovery3 days after operative
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Shanghai Jiao Tong University Affiliated Shanghai Sixth People's Hospital

🇨🇳

Shanghai, Shanghai, China

Shanghai Jiao Tong University Affiliated Shanghai Sixth People's Hospital
🇨🇳Shanghai, Shanghai, China
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