Transverse Abdominis Plane (TAP) Block After Cesarean Delivery
Status: | Recruiting |
---|---|
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | January 2010 |
End Date: | December 2016 |
Contact: | Christopher Cambic, M.D. |
Email: | c-cambic@md.northwestern.edu |
Phone: | 312-926-8373 |
The Postoperative Analgesic Efficacy of Varied Concentrations of Ropivacaine Used for the Transverse Abdominis Plane (TAP) Block After Cesarean Delivery
Cesarean delivery is the most commonly performed surgical procedures in the United States
today, with over 1.2 million cases performed in 2005.1 One of the most important aspects of
cesarean delivery is the provision of safe, effective postoperative analgesia for the
mother, while simultaneously ensuring minimal side effects for both the mother and neonate.
Studies have suggested that a multimodal approach to post-cesarean pain utilizing both
intravenous, oral, and neuraxial opioids and non-steroidal anti-inflammatory drugs is highly
effective in providing effective analgesia.2-4 A significant component of post-cesarean pain
is incisional pain from the Pfannenstiel incision on the anterior abdominal wall. The
sensory supply to the skin, muscles, and parietal peritoneum of the anterior abdominal wall
is derived from the anterior rami of T7-L1. After exiting the spinal column, these nerves
proceed through the lateral abdominal wall within the transversus abdominal fascial plane,
terminating in the anterior abdominal wall.6,7 Recent studies have suggested that blocking
these afferent sensory nerves with local anesthetics, as part of a multimodal postoperative
pain regimen, provides superior pain relief in terms of decreased pain scores and morphine
consumption for up to 48 hours postoperatively.8-10 The technique utilized for these studies
employed a surface anatomical approach to the transversus abdominal fascial plane via the
lumbar triangle of Petit, a technique validated in both cadaveric and radiologic studies.11
However, as ultrasonography has emerged as the "gold standard" for initiating many nerve
blocks, reports have described the successful use of ultrasound imaging for initiation of
transversus abdominis plane (TAP) blocks for both abdominal surgeries and cesarean
deliveries.
In the published studies investigating the use of the TAP block for post-operative
analgesia, either ropivacaine or bupivacaine was utilized in concentrations of 0.75% and
0.375%, respectively. Studies comparing ropivacaine with bupivacaine for use in
interscalene, femoral, or sciatic nerve blocks have found no difference in terms of potency,
time to onset or duration of postoperative analgesia between the two local anesthetics.
Although no similar studies have been done with TAP blocks, one can assume that utilization
of ropivacaine for this nerve block would yield similar results in terms postoperative
analgesia. Moreover, the cardiotoxicity of ropivacaine has been shown to be significantly
less than bupivacaine, making it a safer alternative for use in nerve blocks when used in
high doses.Risk factors for respiratory depression after the administration of neuraxial
opioids in the non-obstetric population include morbid obesity and obstructive sleep apnea.
For the obstetric population, a study of 856 patients revealed that all 8 patients who
experienced respiratory depression after intrathecal morphine for cesarean delivery were
markedly obese. Furthermore, the onset of respiratory depression after intrathecal morphine
can occur up to 12 hours after administration, a time period when the patient is not being
as closely monitored as she is during the 1:1 nursing care in the recovery room. Therefore,
it is the investigators policy on the Labor and Delivery unit to not administer intrathecal
morphine to any parturient with a history of obstructive sleep apnea or a BMI > 40 kg/m2. As
such, these patients often require intravenous opioid patient-controlled analgesia
postoperatively, which has been shown to provide inferior pain relief and greater opioid
consumption than neuraxial opioids. Moreover, the current clinical standard is to administer
the TAP block to those patients who have not received morphine in their neuraxial
anesthetic. Hence, the TAP block offers a novel addition to the management of post-cesarean
pain for this patient population.
Since there have been no published dose-response studies investigating the effective
analgesic dose of ropivacaine for use in a TAP block for post-Cesarean delivery analgesia,
the investigators propose a study primarily examining the effect on 24 hour post-Cesarean
delivery opioid consumption of using either a placebo, 0.25% ropivacaine, 0.5% ropivacaine,
or 0.75% ropivacaine for TAP blocks.
today, with over 1.2 million cases performed in 2005.1 One of the most important aspects of
cesarean delivery is the provision of safe, effective postoperative analgesia for the
mother, while simultaneously ensuring minimal side effects for both the mother and neonate.
Studies have suggested that a multimodal approach to post-cesarean pain utilizing both
intravenous, oral, and neuraxial opioids and non-steroidal anti-inflammatory drugs is highly
effective in providing effective analgesia.2-4 A significant component of post-cesarean pain
is incisional pain from the Pfannenstiel incision on the anterior abdominal wall. The
sensory supply to the skin, muscles, and parietal peritoneum of the anterior abdominal wall
is derived from the anterior rami of T7-L1. After exiting the spinal column, these nerves
proceed through the lateral abdominal wall within the transversus abdominal fascial plane,
terminating in the anterior abdominal wall.6,7 Recent studies have suggested that blocking
these afferent sensory nerves with local anesthetics, as part of a multimodal postoperative
pain regimen, provides superior pain relief in terms of decreased pain scores and morphine
consumption for up to 48 hours postoperatively.8-10 The technique utilized for these studies
employed a surface anatomical approach to the transversus abdominal fascial plane via the
lumbar triangle of Petit, a technique validated in both cadaveric and radiologic studies.11
However, as ultrasonography has emerged as the "gold standard" for initiating many nerve
blocks, reports have described the successful use of ultrasound imaging for initiation of
transversus abdominis plane (TAP) blocks for both abdominal surgeries and cesarean
deliveries.
In the published studies investigating the use of the TAP block for post-operative
analgesia, either ropivacaine or bupivacaine was utilized in concentrations of 0.75% and
0.375%, respectively. Studies comparing ropivacaine with bupivacaine for use in
interscalene, femoral, or sciatic nerve blocks have found no difference in terms of potency,
time to onset or duration of postoperative analgesia between the two local anesthetics.
Although no similar studies have been done with TAP blocks, one can assume that utilization
of ropivacaine for this nerve block would yield similar results in terms postoperative
analgesia. Moreover, the cardiotoxicity of ropivacaine has been shown to be significantly
less than bupivacaine, making it a safer alternative for use in nerve blocks when used in
high doses.Risk factors for respiratory depression after the administration of neuraxial
opioids in the non-obstetric population include morbid obesity and obstructive sleep apnea.
For the obstetric population, a study of 856 patients revealed that all 8 patients who
experienced respiratory depression after intrathecal morphine for cesarean delivery were
markedly obese. Furthermore, the onset of respiratory depression after intrathecal morphine
can occur up to 12 hours after administration, a time period when the patient is not being
as closely monitored as she is during the 1:1 nursing care in the recovery room. Therefore,
it is the investigators policy on the Labor and Delivery unit to not administer intrathecal
morphine to any parturient with a history of obstructive sleep apnea or a BMI > 40 kg/m2. As
such, these patients often require intravenous opioid patient-controlled analgesia
postoperatively, which has been shown to provide inferior pain relief and greater opioid
consumption than neuraxial opioids. Moreover, the current clinical standard is to administer
the TAP block to those patients who have not received morphine in their neuraxial
anesthetic. Hence, the TAP block offers a novel addition to the management of post-cesarean
pain for this patient population.
Since there have been no published dose-response studies investigating the effective
analgesic dose of ropivacaine for use in a TAP block for post-Cesarean delivery analgesia,
the investigators propose a study primarily examining the effect on 24 hour post-Cesarean
delivery opioid consumption of using either a placebo, 0.25% ropivacaine, 0.5% ropivacaine,
or 0.75% ropivacaine for TAP blocks.
Inclusion Criteria:
- ASA II-III patient
- > 18 years of age who is pregnant
- presenting for a cesarean delivery via Pfannenstiel incision who is eligible to
receive a spinal anesthetic with 0.75% bupivacaine and fentanyl and whose is not
eligible to receive intrathecal morphine due to a BMI >40 kg/m2.
Exclusion Criteria:
- < 18 years of age
- contraindication to placement of a spinal anesthetic
- contraindication to use of non-steroidal anti-inflammatory drugs (NSAIDs)
- patients receiving medical therapies considered to result in tolerance to opioids
- patients with a history of established chronic pain, (e.g. chronic low back pain,
fibromyalgia or headaches), defined as requiring regular medical follow-up with pain
specialists, as well as recent use (within the year preceding pregnancy) of opioid
analgesics as an outpatient
- patients with a history of diabetes mellitus
- patients undergoing a vertical midline skin incision
- patients who are undergoing a cesarean delivery after a failed vaginal trial of labor
- patients who had a prior epidural placed for labor analgesia during the same hospital
encounter.
We found this trial at
1
site
303 East Superior Street
Chicago, Illinois 60611
Chicago, Illinois 60611
Principal Investigator: Christopher Cambic, M.D
Phone: 312-926-8373
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