Bilateral Paravertebral Blockade (T7-10) vs. Incisional Local Anesthetic Administration for Pediatric Patients



Status:Completed
Conditions:Post-Surgical Pain
Therapuetic Areas:Musculoskeletal
Healthy:No
Age Range:8 - 17
Updated:11/22/2017
Start Date:November 2010
End Date:May 2013

Use our guide to learn which trials are right for you!

Bilateral Paravertebral Blockade (T7-10) vs. Incisional Local Anesthetic Administration for Laparoscopic Cholecystectomy: a Prospective, Randomized Clinical Study

The objective of this study is to assess the efficacy of paravertebral nerve blocks, single
shot, with ropivacaine 0.5% for postoperative pain control after elective laparoscopic
cholecystectomy as compared with incisional administration of same local anesthetic at
laparoscopic insufflation ports by the surgeon.

Pain after laparoscopic cholecystectomy is a result of many mechanisms such as tissue injury,
local trauma to gallbladder removal, chemical irritation of the peritoneum, pneumoperitoneum.
Effective analgesia in the immediate post-operative period following laparoscopic
cholecystectomy is necessary for optimal recovery. Many methods for pain control after
laparoscopic cholecystectomy have been evaluated, but none of them provided optimal
postoperative analgesia. When used as a complement to general anesthesia, bilateral
paravertebral blockade T5-T6 for adult laparoscopic cholecystectomy has been found to improve
postoperative pain control. Whether this is also the case with pediatric patients is not
certain. Analgesia from administration of local anesthetic by surgeon at insufflations ports
is of short duration and may not provide sufficient pain relief. cholecystectomy.

84 pediatric patients (8-17 yrs old) will be randomly assigned to two groups: Group 1
(treatment group): 42 patients will have six paravertebral nerve blocks with ropivacaine
0.5%, and incisional administration of placebo / normal saline at all four laparoscopic
ports.

Group 2 (control group): 42 patients will have placebo/normal saline in paravertebral space,
same amount, and injection at incision sites for all for insufflation ports with ropivacaine
0.5%.

Both the anesthesiologist and the surgeon will be blinded to patient randomization.

Additional postoperative pain control will be provided via patient administered dilaudid PCA,
for 12 hours after paravertebral block. After PCA is discontinued, the patient will receive
oxycodone po and dilaudid iv for breakthrough pain.

Pain assessment will continue until 24 hours after paravertebral block or patient discharge
if earlier than 24 hours.

The primary end-point of this research is the amount of dilaudid (ng/kg/min) administered via
Patient Controlled Analgesia (PCA), 12 hours after administration of ropivacaine 0.5% /normal
saline in paravertebral space and administration of normal saline/ropivacaine 0.5% at all
four laparoscopic ports.

The secondary end points will be also for total amount of fentanyl (mcg/kg), dilaudid
(mcg/kg), oxycodone (mg/kg) and morphine (mg/kg) (after conversion of above opioids to
morphine based on opioids potency) used intraoperatively and 24 hours postoperatively (or
until the patient is discharged, if sooner).

Postoperative pain scores will be assessed and compared at 4, 8, 12, 18 and 24 hr after
paravertebral block using Visual Analog Scale (VAS).

Other secondary end-points will be possible side effects from opioids administration (nausea,
emesis, itching, and episodes of respiratory depression) and possible complications
associated with nerve blocks: pleural and vascular punctures, pneumothorax, back pain,
bruises, and intravascular administration of local anesthetic.

Inclusion Criteria:

- pediatric patients scheduled for elective laparoscopic cholecystectomy under general
anesthesia

- 8-17 yrs, female and male

- ASA 1, 2, 3

- more than 30 Kg

- BMI less than 36 (to calculate will use http://www.globalrph.com/bmi.htm )

- the patient must be able to self administer opioids via patient control analgesia
(PCA)

- the patient must be able to complete postoperative questionnaires for pain score, pain
type, location, patient satisfaction

- the patient will to be admitted for 24 hrs after surgery

Exclusion Criteria:

- patient refusal

- parental/guardian refusal

- history of coagulopathy, INR more than 1.5, platelets less than 100 000, PT , PTT more
than normal value, patient on Coumadin, heparin or low molecular weight heparin (
LMWH)

- local infection at the planned block site

- vertebral anomalies, (e.g. scoliosis)

- BMI more or equal 36

- patient unable to self administer medications via PCA

- allergy to dilaudid, oxycodone, acetaminophen, ropivacaine

- chronic opioid use

- current weight less than 30 kg

- acute pain (pain on day of surgery that requires pain medication)

- pregnancy test positive
We found this trial at
1
site
4401 Penn Avenue
Pittsburgh, Pennsylvania 15224
412-692-5325
Children's Hospital of Pittsburgh of UPMC UPMC is one of the leading nonprofit health systems...
?
mi
from
Pittsburgh, PA
Click here to add this to my saved trials