Session: 904. Outcomes Research—Non-Malignant Conditions: Poster I
Hematology Disease Topics & Pathways:
Research, Sickle Cell Disease, Translational Research, Hemoglobinopathies, Diversity, Equity, and Inclusion (DEI) , Diseases, Study Population, Human
METHODS: This retrospective cohort study employed an interrupted time series analysis using the IBM® MarketScan® Commercial Database from 1/1/2011 to 12/31/2019. The study population included individuals ≥1 years old who had ≥3 SCD diagnosis codes within 5 years and had no cancer diagnosis. Monthly-measured opioid prescribing levels included: opioid prescription rate, mean daily morphine milligram equivalents (MME) per prescription, and mean number of days supplied per prescription. Health outcomes included: monthly rates of vaso-occlusive crisis (VOC)-related emergency department (ED) visits and hospitalizations, and monthly rates of healthcare facility visits related to opioid use disorder (OUD), depression, and anxiety. Segmented regressions (breakpoint: March 2016) were conducted for all outcomes to compare trends before and after the guideline release.
RESULTS: The study included 14,979 SCD patients (1-65 years old, mean [SD] age = 25.9 [16.9], 56.9% female). After the guideline release, compared to the pre-guideline period, 1) children (1-12 years; N=3,916 [26.4%]) experienced significant decreases in the opioid prescription rate (-0.09 prescription/100 person-month, p=0.001), mean daily MME per prescription (–1.02 MME/month, p=0.001) and the number of days supplied per prescription (-0.02 days/month, p=0.009), but a significant increase in the VOC-related hospitalization rate (+0.11 hospitalizations/100 person-month, p=0.021); 2) adolescents (13-18 years; N=1,782 [11.9%]) experienced significant decreases in the mean daily MME per prescription (-8.48 MME/month, p=0.012) and the number of days supplied (-0.03 days/month, p=0.003), but an increase in the VOC-related hospitalization rate (+0.21 hospitalizations/100 person-month, p=0.003); 3) young adults (19-27 years; N=2,599 [17.4%]) experienced a significant decrease in the number of days supply (-0.04 days/month, P<0.001), and no significant change in the VOC-related outcomes; 4) adults 28-45 years (N=4,293 [28.7%]) experienced significant decreases in opioid prescription rate (-0.48 prescription/100 person-month, p<0.001), mean daily MME per prescription (–21.19 MME/month, p<0.001), and the number of days supplied (-0.06 days/month, p<0.001), but significant increases in VOC-related ED visit rate (+0.13 visits/month, p<0.001) and hospitalization rate (+0.30 hospitalizations/100 person-month, p<0.001); and 5) adults 46-65 years (N=2,344 [15.6%]) experienced significant decreases in the opioid prescription rate (-0.55 prescription/100 person-month, p<0.001), mean daily MME per prescription (-3.68 MME/month, p<0.001), the number of days supplied (-0.03 days/month, p=0.003), and VOC-related ED visit rate (-0.1 visits/100 person-months, p=0.023). OUD-related healthcare facility visits did not differ in either pediatric (1-18 years) or adult (19-65 years) patients before vs. after the guideline release. Depression-related visits increased significantly (+0.09 visits/100 person-months, p=0.002) among adult patients while anxiety-related visits decreased significantly (-0.05 visits/100 person-months, p=0.023) among the same population post-guideline compared to the pre-guideline periods.
CONCLUSIONS: The CDC guideline release was associated with a decrease in opioid prescribing levels across all age groups even though the guideline was intended only for the adult population. Overall, pain-related health outcomes were negatively impacted by the guideline: older age groups with increased ED visits and younger age groups with increased hospitalizations, while there were no decreases in the rate of OUD.
Disclosures: Ataga: Pfizer: Consultancy; Roche: Consultancy; Biomarin: Consultancy; Agios Pharmaceuticals: Consultancy; Forma Therapeutics: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding.
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