Shared Decision Making for Prescription Opioids After Cesarean Delivery
Status: | Completed |
---|---|
Conditions: | Women's Studies |
Therapuetic Areas: | Reproductive |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/9/2019 |
Start Date: | April 2016 |
End Date: | September 2016 |
The specific aim of this study is to use a shared decision making tool to allow women who
have undergone cesarean delivery (CD) to choose the amount of oxycodone the participants will
be prescribed at discharge, within a range from 0-40 tablets. The study investigators will
document additional information from medical record abstraction (age, race/ethnicity, medical
and obstetrical conditions, previous opioid use, date of CD, indication for CD, anesthetic
management during CD, duration and complications of CD, length of stay, pain medication use
and pain scores on each postoperative day between CD and discharge). The investigators will
then follow up with the participants by telephone at two weeks after discharge to assess the
amount of opioid used, frequency of prescription refill, disposition of unused medication,
and participant satisfaction with their post-cesarean pain control. The investigators
hypothesize that the use of a shared decision making tool will decrease the amount of opioid
prescribed while still providing participants with satisfactory pain control.
have undergone cesarean delivery (CD) to choose the amount of oxycodone the participants will
be prescribed at discharge, within a range from 0-40 tablets. The study investigators will
document additional information from medical record abstraction (age, race/ethnicity, medical
and obstetrical conditions, previous opioid use, date of CD, indication for CD, anesthetic
management during CD, duration and complications of CD, length of stay, pain medication use
and pain scores on each postoperative day between CD and discharge). The investigators will
then follow up with the participants by telephone at two weeks after discharge to assess the
amount of opioid used, frequency of prescription refill, disposition of unused medication,
and participant satisfaction with their post-cesarean pain control. The investigators
hypothesize that the use of a shared decision making tool will decrease the amount of opioid
prescribed while still providing participants with satisfactory pain control.
Inclusion Criteria:
- Postpartum women who underwent a cesarean delivery at MGH
Exclusion Criteria:
- Non-native English speakers (identified in LMR as "non-English speaking" or "requires
interpreter")
- Women with a history of chronic opioid abuse (identified in LMR as "opioid abuse" or
"narcotic abuse")
- Chronic pain on opioids (identified in LMR as "chronic pain" or "chronic narcotic
use")
- Women on methadone or buprenorphine for treatment of opioid addiction (identified from
their medication list in the LMR)
- Women with impaired decision-making abilities
- Women hospitalized for > 7 days related to CD
- Minors (<18 years old)
- Women being prescribed an opioid other than oxycodone during their postpartum
hospitalization (identified from the MAR and discussion with rounding providers)
- Women with contraindications to taking acetaminophen or NSAIDs
We found this trial at
1
site
185 Cambridge Street
Boston, Massachusetts 02114
Boston, Massachusetts 02114
617-724-5200
Phone: 617-529-7058
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