Hip Arthroplasty Clinical Trial
Official title:
Peripheral Nerve Block vs Spinal Anesthesia in Hip Surgery: a Randomized Study
Anesthesia plays an important role in the patient's outcome: each anesthesiological technique
has a different cardiovascular impact, because they act differently on the autonomic nervous
system, which in turn regulates heart rate, myocardial contractility and vascular tone.
Subarachnoid anesthesia can result in a reduction in cardiac output, hypotension and
bradycardia due to blockage of the nerve fibers of the sympathetic system, while peripheral
nerve block is associated with a lower impact on the autonomic nervous system, therefore less
influence on hemodynamic changes compared to subarachnoid anesthesia.
Hypotension can lead to myocardial ischaemia, especially in patients at high surgical risk.
In addition, peripheral nerve block allows for better coverage from postoperative pain
compared to subarachnoid anesthesia in patients undergoing hip surgery.
This leads to less postoperative stress, with less impact on cardiac and respiratory
function.
Numerous studies have shown the efficacy and safety of regional anesthesia in hip surgery.
This study aims to compare the hemodynamic changes of subarachnoid anesthesia and peripheral
nerve block in patients who underwent total and partial hip replacement
All patients who meet the inclusion and exclusion criteria will be enrolled. Enrolled
patients will be informed of the study modality. In case of a favorable opinion, the patient
will be made to sign the informed consent. Subsequently a code will be assigned to the
patient for randomization.
There are two randomization groups: in the PNB group the patient will undergo lumbar plexus
block, sciatic nerve block, lateral femoral cutaneous nerve block and lateral branch of
iliohypogastric nerve block, while in the SA group, the patient will undergo subarachnoid
anesthesia and lumbar plexus block.
In the preoperative room, ECG, pulseoximetry will be estabilished and an arterial radial
cannula will be inserted under local anesthesia to monitor blood pressure. A premedication
with midazolam (0.05-0.1 mg / kg) will be administered before anesthesia is performed.
At this point, the type of anesthesia will be followed on the basis of the randomization
group.
The following variables will be evaluated:
- hemodynamic parameters in the perioperative period
- onset time of the sensory and motor block
- fluids and vasoactive drugs administered
- anesthesiological complications
- degree of patient satisfaction
- duration of surgery
- degree of postoperative pain and analgesic therapy administered
- mini mental state evaluation (in the preoperative and postoperative period)
- start physical rehabilitation
- clinical complications during hospitalization
- duration of hospitalization
;
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