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Comparison of IV PCA and Wound Infusion After Repair of Pectus Excavatum

Phase 4
Completed
Conditions
Pain
Side Effects
Interventions
Device: IV PCA
Device: Continuous wound infusion
Registration Number
NCT01908491
Lead Sponsor
The Catholic University of Korea
Brief Summary

Postoperative pain management is a major problem after repair of pectus excavatum.Various methods of pain management have been introduced. However, the effects of continuous wound infusion of local anesthetics through ON-Q catheters were not well evaluated in pectus surgery. Therefore, we conducted prospective randomized controlled study to compare the effects of IV PCA and continuous wound infusion after repair of pectus excavatum.

Detailed Description

Pain control is an important issue after correction of pectus excavatum. Insufficient pain control leads to develop postoperative pulmonary complications, such as hypoxia, atelectasis and pneumonia. Additionally, hospital length of stay could be prolonged. Therefore, successful pain management is mandatory to improve clinical outcome, to decrease postoperative morbidity and to shorten the duration of hospital stay. Various methods of pain management have been introduced. Current typical methods for pain management include thoracic epidural analgesia and intravenous patient-controlled analgesia (IV PCA). Epidural analgesia has shown superior pain control effects. However, there may be rare but serious complications, such as spinal cord and nerve root lesions, epidural hematoma, or infections. IV PCA is a well-established method of postoperative pain management. However, the systemic side effects of opioid, such as nausea, vomiting, sedation, or respiratory depression may occur. Continuous wound infusion of local anesthetics through ON-Q catheters is another method for pain management. It has been used for various surgical procedures. However, the effect is not well evaluated in pectus surgery. The purpose of this study is to compare the effects of opioid-based IV PCA and continuous wound infusion using a catheter.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
80
Inclusion Criteria
  • patients undergoing the repair of pectus excavatum
Exclusion Criteria
  • allergy to opioid or local anesthetics
  • reoperation

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
IV PCAIV PCAhydromorphone with ketorolac
Continuous wound infusionContinuous wound infusionON-Q Painbuster with ropivacaine
Primary Outcome Measures
NameTimeMethod
Changes of pain scoreduring 48 hours after surgery

Pain score was measured by the Wong-Baker FACES pain scale at 1, 2, 6, 24, 48 hours after surgery. Pain scale consists of 6 faces with word descriptors and numbers from 0 to 10. The child look at the faces, the nurse or parent uses the words to describe the expression, and the child is asked to point to the face that describes how he/she feels. The number is used to record a pain score. This simple and quick scale can be easily reproduced for use at the bed-side with children as young as 3 years of age.

Secondary Outcome Measures
NameTimeMethod
Incidence of side effectsduring 48 hours after surgery

Number of patients who developed nausea, vomiting, sedation, respiratory depression,or wound catheter related complications are recorded.

Trial Locations

Locations (1)

Seoul St. Mary's Hospital, the Catholic University of Korea

🇰🇷

Seoul, Korea, Republic of

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