TY - JOUR
T1 - Impact of a tiered discharge opioid algorithm on prescriptions and patient-reported outcomes after open gynecologic surgery
AU - Huepenbecker, Sarah
AU - Hillman, Robert Tyler
AU - Iniesta, Maria D.
AU - Chen, Tsun
AU - Cain, Katherine
AU - Mena, Gabriel
AU - Lasala, Javier
AU - Wang, Xin Shelley
AU - Williams, Loretta
AU - Taylor, Jolyn S.
AU - Lu, Karen H.
AU - Ramirez, Pedro T.
AU - Meyer, Larissa A.
N1 - Funding Information:
Competing interests LAM reports research funding from AstraZeneca, consulting for GlaxoSmithKline, and stocks in Crispr and Bristol-Myers Squibb. LW reports grants from AstraZeneca, Astellas, Bayer, Bristol Meyers Squibb, Genentech, Merck, and Eli Lily. GM reports a research/academic grant from PACIRA Pharmaceutical.
Funding Information:
Funding This work was supported in part by the MD Anderson Cancer Center Support Grant from the National Cancer Institute of the National Institutes of Health (NIH/NCI P30 CA016672, CA217685) and the T32 training grant CA101642 (SPH). LAM is supported by a NIH-NCIK07-CA201013 grant. XSW is supported by NCI/ NIH “Improving Recovery After Major Cancer Surgery Using Patient-Reported Outcomes”, R01CA205146.
Publisher Copyright:
© 2021 BMJ Publishing Group. All rights reserved.
PY - 2021/7/1
Y1 - 2021/7/1
N2 - Objective To compare discharge opioid refills, prescribed morphine equivalent dose and quantity, and longitudinal patient-reported outcomes before and after implementation of a tiered opioid prescribing algorithm among women undergoing open gynecologic surgery within an enhanced recovery after surgery program. Methods We compared opioid prescriptions, clinical outcomes, and patient-reported outcomes among 273 women. Post-discharge symptom burden was collected up to 42 days after discharge using the validated 27-item MD Anderson Symptom Inventory and analyzed using linear mixed effects models and Kaplan-Meier curves for symptom recovery. Results Among 113 pre-implementation and 160 post-implementation patients there was no difference in opioid refills (9.7% vs 11.3%, p=0.84). The post-implementation cohort had a significant reduction in median morphine equivalent dose (112.5 mg vs 225 mg, p<0.01), with no difference in median hospital length of stay (3 days vs 3 days, p=1.0) or 30-day readmission rate (9.4% vs 7.1%, p=0.66). There was no difference in patient-reported pain between the pre- and post-implementation cohorts on the day of discharge (severity 4.93 vs 5.14, p=0.53) or in any patient-reported symptoms, interference measures, or composite scores by post-discharge day 7. The median recovery time for most symptoms was 7 days, except for pain (14 days), fatigue (18 days), and physical interference (21 days), with no differences between cohorts. Conclusions After implementation of a tiered opioid prescribing algorithm, the quantity and dose of discharge opioids prescribed decreased with no change in post-operative refills and without negatively impacting patient-reported symptom burden or interference, which can be used to educate and reassure patients and providers.
AB - Objective To compare discharge opioid refills, prescribed morphine equivalent dose and quantity, and longitudinal patient-reported outcomes before and after implementation of a tiered opioid prescribing algorithm among women undergoing open gynecologic surgery within an enhanced recovery after surgery program. Methods We compared opioid prescriptions, clinical outcomes, and patient-reported outcomes among 273 women. Post-discharge symptom burden was collected up to 42 days after discharge using the validated 27-item MD Anderson Symptom Inventory and analyzed using linear mixed effects models and Kaplan-Meier curves for symptom recovery. Results Among 113 pre-implementation and 160 post-implementation patients there was no difference in opioid refills (9.7% vs 11.3%, p=0.84). The post-implementation cohort had a significant reduction in median morphine equivalent dose (112.5 mg vs 225 mg, p<0.01), with no difference in median hospital length of stay (3 days vs 3 days, p=1.0) or 30-day readmission rate (9.4% vs 7.1%, p=0.66). There was no difference in patient-reported pain between the pre- and post-implementation cohorts on the day of discharge (severity 4.93 vs 5.14, p=0.53) or in any patient-reported symptoms, interference measures, or composite scores by post-discharge day 7. The median recovery time for most symptoms was 7 days, except for pain (14 days), fatigue (18 days), and physical interference (21 days), with no differences between cohorts. Conclusions After implementation of a tiered opioid prescribing algorithm, the quantity and dose of discharge opioids prescribed decreased with no change in post-operative refills and without negatively impacting patient-reported symptom burden or interference, which can be used to educate and reassure patients and providers.
KW - gynecologic surgical procedures
KW - opioid-related disorders
KW - postoperative care
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U2 - 10.1136/ijgc-2021-002674
DO - 10.1136/ijgc-2021-002674
M3 - Article
C2 - 34135073
AN - SCOPUS:85108544885
SN - 1048-891X
VL - 31
SP - 1052
EP - 1060
JO - International Journal of Gynecological Cancer
JF - International Journal of Gynecological Cancer
IS - 7
ER -