Patient Controlled Oral Analgesia for Postoperative Pain Management After Total Knee Replacement
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Purpose
Patient Centered Care (PCC) is "an approach that consciously adopts the patient's perspective...about what matters" (Gerteis, Edgeman, Levitan, Walker, Stokes, Cleary, Delbanco, 1993). Experiencing pain is the most common concern of patients before surgery - even ahead of whether the surgery would improve their condition (Apfelbaum, 2003). Current standard of practice for post-operative pain management in most acute care hospitals today is intravenous patient controlled analgesia (IV PCA). However, despite the fact that patients prefer IV PCA because it affords them greater control and provides them with better pain relief (Ballantyne, Carr, deFerranti, Suarez, Lau, Chalmers, Angelillo, Mosteller, 1998 ; Rawal, 2001), hospitals routinely take control of pain medications away from patients once they are switched to pain tablets. Patients must then wait, in pain, for their nurse to bring them pain tablets.
Patient controlled oral analgesia (PCOA) has been utilitzed in several centers in the US and Germany. Preliminary evidence from the literature seems to indicate that the benefits of PCOA are similar to IV PCA including increased patient satisfaction and better pain control (Striebel, Romer, Kopf, Schwagmeier ,1996; Striebel, Scheitza, Philippi, Behrens, Toussaint, 1998). At the Toronto Western Hospital, University Health Network, we have successfully implemented a PCOA program on two surgical units (Orthopedics/Rheumatology and Spinal). The purpose of this study is to compare usual nurse administered oral analgesia to PCOA with respect to pain, patient satisfaction, and passive range of knee motion in postoperative total knee replacement patients.
| Condition | Intervention |
|---|---|
|
Self-Administered Versus Nurse Administered Pain Medication. |
Behavioral: Self-administration or nurse administered medication |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Patient Controlled Oral Analgesia (PCOA) for Postoperative Pain Management After Total Knee Replacement-A Pilot Study |
Eligibility| Ages Eligible for Study: | 18 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- able to read and write English
- post elective total knee replacement surgery (primary or revision)
- already on IV PCA
- age 18-80
- able to tolerate oral medication
- able to physically open a childproof vial independently (including the absence of any significant problems with manual power, dexterity or visual acuity)
- able and willing to complete Oral PCA flowsheet
Exclusion Criteria:
- history of substance abuse
- history of sleep apnea
- episode(s) of confusion, disorientation during this admission
- episode(s) of respiratory depression during this admission
- history of major psychiatric disorder pregnancy
Contacts and Locations| Canada, Ontario | |
| Universtiy Health Network | |
| Toronto, Ontario, Canada, M5T 2S8 | |
| University Health Network | |
| Toronto, Ontario, Canada, M5T 2S8 | |
| Toronto Western Hospital | |
| Toronto, Ontario, Canada, M5T 2S8 | |
| Principal Investigator: | Patti Kastanias, RN, MSc(A), ACNP | University of Health Network, Toronto |
More Information
No publications provided
| Responsible Party: | Patti Kastanias, University Health Network |
| ClinicalTrials.gov Identifier: | NCT00221936 History of Changes |
| Other Study ID Numbers: | UHN04-0394-AE |
| Study First Received: | September 20, 2005 |
| Last Updated: | December 4, 2008 |
| Health Authority: | Canada: UHNToronto |
Additional relevant MeSH terms:
|
Pain, Postoperative Postoperative Complications Pathologic Processes Pain Signs and Symptoms |
ClinicalTrials.gov processed this record on May 23, 2013