Abstract
Objective:
In non-steroidal anti-inflammatory drug (NSAID) users, chronic occult blood loss may lead to decreases in hemoglobin, which may lead to increased healthcare expenditures. This study, therefore, sought to quantify healthcare resource utilization of ≥2 g/dL hemoglobin decrease in osteoarthritis patients.
Methods:
Using a large US managed care database, osteoarthritis patients aged ≥18 years who had exposure to ≥90 days of non-selective or selective COX-2 NSAID use, a hemoglobin value within 6 months before index NSAID, and at least one hemoglobin value 24 months after were evaluated. Resource utilization was evaluated in those with ≥2 g/dL hemoglobin drop vs patients with ≤0.5 g/dL hemoglobin drop (control).
Results:
Of 1800 NSAID users meeting inclusion criteria, 228 patients [mean (SD) = 59.8 (9.3) years] had ≥2 g/dL hemoglobin drop vs 1572 controls [mean (SD) = 58.3 (8.0) years]. Despite relatively low absolute rates, endoscopic procedures were more commonly observed in the ≥2 g/dL hemoglobin drop group [endoscopy: 37/228 (16.2%) vs 65/1572 (4.1%); adjusted odds ratio (AOR) 3.5, (95% confidence interval [CI] = 2.1–6.0); colonoscopy: 36/228 (15.8%) vs 137/1572 (8.7%); AOR 2.0 (95% CI 1.2–3.2)]. During the 12-month follow-up, patients with ≥2 g/dL hemoglobin drop utilized significantly more healthcare resources [adjusted relative risk (95% CI) for hospitalization, 2.1 (1.5–2.9); outpatient visits, 1.4 (1.3–1.5); physician visits, 1.3 (1.1–1.4)] and charges (total adjusted charges $47,766 vs $23,342) across major categories of healthcare services.
Limitations:
This was a retrospective analysis with baseline demographic differences. The source or cause of the hemoglobin drops could not be verified; and it is assumed that they are related to occult gastrointestinal loss. Differences with healthcare utilization and charges were not linked to hemoglobin-associated complications.
Conclusion:
In patients exposed to NSAIDs, those with significant hemoglobin drops experienced higher subsequent healthcare utilization and charges than controls who did not have a significant hemoglobin drop.
Transparency
Declaration of funding
The study was funded in full by Pfizer Inc.
Declaration of financial/other relationships
JLG has served as a speaker for Pfizer, AstraZeneca, and Takeda, as a consultant for Pfizer, AstraZeneca, Takeda, Logical Therapeutics, Novartis, Astellas, GlaxoSmithKline, Proctor and Gamble, and Pozen, and has received research funding from Pfizer, AstraZeneca, Logical Therapeutics, Pozen, and Sucampo. XL, JCC, and GHS are employees of Pfizer Inc and all own stocks and shares in Pfizer Inc. JME Peer Reviewers on this manuscript have no relevant financial relationships to disclose.
Acknowledgments
Writing support was provided by C. Campbell, PhD, of PAREXEL, and was funded by Pfizer Inc.