Evaluation of Post-PACU Pain Management in Pediatric Surgery
Status: | Recruiting |
---|---|
Conditions: | Chronic Pain |
Therapuetic Areas: | Musculoskeletal |
Healthy: | No |
Age Range: | 1 - 6 |
Updated: | 2/2/2019 |
Start Date: | June 2013 |
End Date: | December 2022 |
Contact: | Lena Sun, MD |
Phone: | 212-305-2413 |
Evaluation of Post-PACU Pain Management Experiences in Pediatric Ambulatory Surgery Patients
This study aims to assess the differences in overall pain severity, pain management, and
satisfaction during recovery period between two groups of children who either receive or do
not receive additional education related to expectation and management of postoperative pain.
satisfaction during recovery period between two groups of children who either receive or do
not receive additional education related to expectation and management of postoperative pain.
With the increased frequency and popularity of pediatric ambulatory surgery, there is a
greater need for evaluation of the postoperative pain experience after discharge from the
hospital. Pain is one of the most significant factors affecting the postoperative experience
in adults, and also be true in the pediatric population. Control of postoperative pain in
children after discharge from the hospital poses particular challenges due to dependence on
parental or caretaker ability to properly evaluate the child's pain, their understanding of
appropriate dosing of pain medications, and their willingness to administer enough
medications until sufficient relief is achieved.
The investigators aim to assess the differences in reported pain between groups who receive
additional face-to-face education versus the current standard of care at a major US teaching
hospital. The study will assess pain management after surgery using parental reports and
questionnaires to assess their child's pain at multiple time points during the study.
Additionally, this study will also assess baseline behavioral attributes of children and will
compare behavioral changes at 24-48 hours, 7-10 days, and 2-4 weeks postoperatively as these
behavior changes may also affect overall postoperative experience.
This study is divided into phase I and phase II. Phase I is the initial assessment of the
investigators' institution's pain management in healthy pediatric patients undergoing
ambulatory surgical procedures. Phase II consists of randomized trial which includes a
randomized intervention group and control group. The group selected randomly for intervention
will receive additional teaching regarding what to expect in terms of postoperative pain and
how to properly identify pain in children.
greater need for evaluation of the postoperative pain experience after discharge from the
hospital. Pain is one of the most significant factors affecting the postoperative experience
in adults, and also be true in the pediatric population. Control of postoperative pain in
children after discharge from the hospital poses particular challenges due to dependence on
parental or caretaker ability to properly evaluate the child's pain, their understanding of
appropriate dosing of pain medications, and their willingness to administer enough
medications until sufficient relief is achieved.
The investigators aim to assess the differences in reported pain between groups who receive
additional face-to-face education versus the current standard of care at a major US teaching
hospital. The study will assess pain management after surgery using parental reports and
questionnaires to assess their child's pain at multiple time points during the study.
Additionally, this study will also assess baseline behavioral attributes of children and will
compare behavioral changes at 24-48 hours, 7-10 days, and 2-4 weeks postoperatively as these
behavior changes may also affect overall postoperative experience.
This study is divided into phase I and phase II. Phase I is the initial assessment of the
investigators' institution's pain management in healthy pediatric patients undergoing
ambulatory surgical procedures. Phase II consists of randomized trial which includes a
randomized intervention group and control group. The group selected randomly for intervention
will receive additional teaching regarding what to expect in terms of postoperative pain and
how to properly identify pain in children.
Inclusion Criteria:
- Patients ages 1-6 years undergoing ambulatory surgical procedures.
- Patients with an ASA status of I or II spending 23 hours or less recovering in the
PACU and discharged home.
Exclusion Criteria:
- Patients with an ASA status of III or IV.
- Patients admitted as inpatients or transferred to the PICU or inpatient for recovery,
and any conditions that may affect pain expression or sensation.
We found this trial at
1
site
116th St and Broadway
New York, New York 10027
New York, New York 10027
(212) 854-1754
Phone: 212-305-2413
Columbia University In 1897, the university moved from Forty-ninth Street and Madison Avenue, where it...
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