patients who receive hip arthoplasty, including total hip arthroplasty, hemiarthroplasty
Conditions
Interventions
PENG block
Sponsors
Jin Zhuan
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Eligible studies included prospectively registered clinical trials in forms of articles on peer-reviewed journals, letters, or conference abstracts, where (1) adult patients who received any types of hip arthroplasty under either general or spinal anesthesia; (2) patients were allocated to PENG block (including ultrasound-guided, X-ray-guided, CT-guided or traditional landmark-based techniques) as an intervention compared with any other kind of analgesia management other than PENG block for perioperative pain management. No language restrictions were applied. Studies published as Non-English, Chinese, Japanese studies were translated using an online translator.
Exclusion criteria
Exclusion criteria: Exclusion criteria include: (1) studies that had another block as a co-intervention, except for lateral femoral cutaneous nerve (LFCN) block or infiltration using local anesthetics; (2) studies of catheter-based continuous blocks; (3) studies where both intervention and comparison were PENG block; (4) studies with data that could not be used for statistical analysis, or studies with incomplete data, or data that could not be extracted after contacting the original authors; and (5) studies that were duplicate publications, or not prospectively registered.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| QoR-15, QoR-40 score on POD1 (evaluated within 24 hours from surgery, on postoperative day 1, or on the second day of surgery) | — |
Secondary
| Measure | Time frame |
|---|---|
| (1) QoR-15 score reported in other time frame: 48 hours or on POD2, etc. (2) QoR-40 score reported in any time frame: POD1, POD2, etc. (3) Time to first mobilization: the time from the end of surgery to the first mobilization, ambulation, walk, or getting up from bed (4) First ambulation distance (5) First up-and-go test (6) Quadriceps strength on POD1 (7) Other evaluation tool of recovery or patient-reported outcomes, such as the Hip disability and Osteoarthritis Outcome Score for Joint Replacement (HOOS, JR.), the Patient-Reported Outcomes Measurement Information System (PROMIS) (8) Patient satisfaction: any satisfaction questionnaire results with perioperative pain management techniques or postoperative analgesia evaluated on a certain scale were included (9) Postoperative complications reported if possible | — |
Contacts
Public ContactZhuan Jin
Kameda Medical Center
Outcome results
None listed