Lumbar Plexus Block vs Fascia Iliaca Block After Hip Arthroscopy
Status: | Recruiting |
---|---|
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/17/2018 |
Start Date: | November 2015 |
End Date: | December 2018 |
Contact: | Rebekah Williams |
Email: | anesthesiaresearch@uphs.upenn.edu |
Phone: | 215-294-9165 |
Lumbar Plexus Block vs Fascia Iliaca Block After Hip Arthroscopy: A Non-inferiority Study
The purpose of this study is to compare lumbar plexus block to fascia iliac block done in
adult patients who have undergone hip arthroscopy surgery. Visual analogue scores, opioid
consumption, and quality of recovery 48 hours post operatively will be used for comparison.
adult patients who have undergone hip arthroscopy surgery. Visual analogue scores, opioid
consumption, and quality of recovery 48 hours post operatively will be used for comparison.
If the patient is willing to participate and signs the consent, he/she will be randomized to
one of the two treatment groups:
1. Lumbar Plexus Block
2. Fascia Iliaca Block
The patient will undergo general anesthesia as by the attending anesthesiologist assigned to
the case. No intraoperative restrictions will be required for this study. Once in the PACU,
the patient will be assessed and if their pain score is ≥ 4 on the NRS, the patient will be
randomized to a lumbar plexus block or fascia iliaca block.
Patients will be monitored during block performance with standard ASA monitors. All patients
will receive 2 L of oxygen via a nasal cannula. Sedatives will be titrated to effect.
Midazolam 1-2 mg, and fentanyl 50-100 mcg will be used for sedation.
The fascia iliaca block will be performed in a standard fashion as described2. The patient
will be placed in a supine position. The ipsilateral groin will be prepped and cleaned with
chlorhexidine. An ultrasound machine with a linear transducer covered with a sterile tegaderm
will be utilized. The transducer is placed inferior to the inguinal ligament until the
femoral artery is located. The probe is then moved laterally until the Sartorius muscle is
seen. A skin wheal with 3ml of 1% lidocaine is made and a 2-inch blunt tip needle is inserted
in plane. The needle is seen to pierce the fascia iliaca and 1-2 ml of 0.25% Preservative
Free bupivacaine with 1:200,000 epinephrine is injected to confirm correct needle placement
between the fascia iliaca and iliopsoas muscle. An injection will be deemed adequate if local
anesthetic is seen to separate these two layers in a medial to lateral direction. A total of
30ml of the above solution will be injected.
The lumbar plexus block will be performed with the patient placed in a lateral position with
the operative side facing up. An ultrasound machine with a curved transducer covered with a
sterile tegaderm will be utilized. The ipsilateral hip and knee will be flexed to 90 degrees.
The anatomy for the LP block will be localized using a modified transverse scan of the lumbar
paravertebral area (PMTS). This technique is well described by Karmarkar et al.7 The target
vertebral level will be identified by locating the lumbosacral junction (the gap of L5-S1)
using a paramedian sagittal scan and then counting cranially to locate both the lamina and
the transverse process of L3-L5. The transducer is then placed 4 cm lateral to the midline at
the L3-4 level and directed medially to insonate the intervertebral foramen through the
lumbar intervertebral space. A skin wheal is made at this site with 1% lidocaine. and a 4
inch blunt tip needle is introduced 4 cm lateral to the midline and just medial of the
transducer after connecting it to a nerve stimulator set at 1.00 mA. The needle is slowly
advanced under ultrasound guidance until engaged in the psoas compartment and a quadriceps
twitch is elicited. The nerve stimulator is turned down until the twitch is abolished at
0.3mA or less. 1-2cmlof 0.25% Preservative free Bupivacaine with 1:200,000 epinephrine is
injected slowly after negative aspiration. A total of 30ml will be injected. Spread will be
confirmed with ultrasound.
All patients will receive prophylaxis for postoperative nausea and vomiting (PONV) during
surgery. The protocol for prophylaxis against PONV includes administration of 4 mg of
dexamethasone after induction of anesthesia and 4 mg of ondansetron 20 minutes before
recovery from anesthesia. Dexamethasone is withheld if the patient has poorly controlled
diabetes mellitus (DM). Uncontrolled DM will be defined as random blood glucose above 250
mg/dl.
one of the two treatment groups:
1. Lumbar Plexus Block
2. Fascia Iliaca Block
The patient will undergo general anesthesia as by the attending anesthesiologist assigned to
the case. No intraoperative restrictions will be required for this study. Once in the PACU,
the patient will be assessed and if their pain score is ≥ 4 on the NRS, the patient will be
randomized to a lumbar plexus block or fascia iliaca block.
Patients will be monitored during block performance with standard ASA monitors. All patients
will receive 2 L of oxygen via a nasal cannula. Sedatives will be titrated to effect.
Midazolam 1-2 mg, and fentanyl 50-100 mcg will be used for sedation.
The fascia iliaca block will be performed in a standard fashion as described2. The patient
will be placed in a supine position. The ipsilateral groin will be prepped and cleaned with
chlorhexidine. An ultrasound machine with a linear transducer covered with a sterile tegaderm
will be utilized. The transducer is placed inferior to the inguinal ligament until the
femoral artery is located. The probe is then moved laterally until the Sartorius muscle is
seen. A skin wheal with 3ml of 1% lidocaine is made and a 2-inch blunt tip needle is inserted
in plane. The needle is seen to pierce the fascia iliaca and 1-2 ml of 0.25% Preservative
Free bupivacaine with 1:200,000 epinephrine is injected to confirm correct needle placement
between the fascia iliaca and iliopsoas muscle. An injection will be deemed adequate if local
anesthetic is seen to separate these two layers in a medial to lateral direction. A total of
30ml of the above solution will be injected.
The lumbar plexus block will be performed with the patient placed in a lateral position with
the operative side facing up. An ultrasound machine with a curved transducer covered with a
sterile tegaderm will be utilized. The ipsilateral hip and knee will be flexed to 90 degrees.
The anatomy for the LP block will be localized using a modified transverse scan of the lumbar
paravertebral area (PMTS). This technique is well described by Karmarkar et al.7 The target
vertebral level will be identified by locating the lumbosacral junction (the gap of L5-S1)
using a paramedian sagittal scan and then counting cranially to locate both the lamina and
the transverse process of L3-L5. The transducer is then placed 4 cm lateral to the midline at
the L3-4 level and directed medially to insonate the intervertebral foramen through the
lumbar intervertebral space. A skin wheal is made at this site with 1% lidocaine. and a 4
inch blunt tip needle is introduced 4 cm lateral to the midline and just medial of the
transducer after connecting it to a nerve stimulator set at 1.00 mA. The needle is slowly
advanced under ultrasound guidance until engaged in the psoas compartment and a quadriceps
twitch is elicited. The nerve stimulator is turned down until the twitch is abolished at
0.3mA or less. 1-2cmlof 0.25% Preservative free Bupivacaine with 1:200,000 epinephrine is
injected slowly after negative aspiration. A total of 30ml will be injected. Spread will be
confirmed with ultrasound.
All patients will receive prophylaxis for postoperative nausea and vomiting (PONV) during
surgery. The protocol for prophylaxis against PONV includes administration of 4 mg of
dexamethasone after induction of anesthesia and 4 mg of ondansetron 20 minutes before
recovery from anesthesia. Dexamethasone is withheld if the patient has poorly controlled
diabetes mellitus (DM). Uncontrolled DM will be defined as random blood glucose above 250
mg/dl.
Inclusion Criteria:
- Adult patients18 years and older scheduled for hip arthroscopy surgery
- American Society of Anesthesiologists (ASA) physical status I -III
- Mentally competent and able to give consent for enrollment in the study
Exclusion Criteria:
- Chronic opioid use (use of any opioid daily or on most days of the week for more than
3 months)
- Diagnosed peripheral neuropathy in the surgical lower extremity
- Allergy to study medications
- BMI >42
We found this trial at
1
site
3451 Walnut St
Philadelphia, Pennsylvania 19104
Philadelphia, Pennsylvania 19104
1 (215) 898-5000
Principal Investigator: Ignacio Badiola, MD
Phone: 215-294-9165
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