Resumen
Objective To identify predictors of the receipt of medical care, including the receipt of pre-drug screening, for diagnostically targeted fungal or mycobacterial infections among patients prescribed a tumor necrosis factor inhibitor (TNFi). Methods We conducted a case-control study using deidentified patient health claims information from a data set representing a commercially insured US population of 15 million patients annually from January 1, 2007 to December 31, 2009. Descriptive statistics as well as a 2-sample t-test, chi-square test of association, Fisher's exact test, and multivariate logistic regression were used for data analysis. Results A total of 30,772 patients received a TNFi during the study period. Of these, 158 patients (0.51%) developed targeted fungal and/or mycobacterial infections (cases). The median number of infections per case was 1.0 (interquartile range 1.0-2.0). Tuberculosis was diagnosed in 61% of cases, followed by histoplasmosis in 60%, nontuberculous mycobacterial infections in 11%, coccidioidomycosis in 10%, unspecified fungal infection in 8%, blastomycosis in 4%, cryptococcal infection in 3%, and pneumocystosis in 2%. Compared to controls (n = 474), a higher proportion of cases were prescribed prednisone (55% versus 37%; P < 0.001). Patients who were prescribed prednisone during the study period were twice as likely as those not taking prednisone to seek medical care attributable to a targeted fungal or mycobacterial infection (odds ratio 2.03; P < 0.001). Conclusion Development of a targeted fungal or mycobacterial infection among patients taking a TNFi is rare. Concomitant use of prednisone predicted development of such infections.
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 597-603 |
| Número de páginas | 7 |
| Publicación | Arthritis and Rheumatology |
| Volumen | 68 |
| N.º | 3 |
| DOI | |
| Estado | Published - mar 1 2016 |
Nota bibliográfica
Funding Information:Drs. Salt and Huaman's work was supported in part by the National Center for Research Resources (NCRR) and the National Center for Advancing Translational Sciences, NIH (grant UL1-TR-000117). Access to the large commercially insured data set was made available with funding from the Clinical and Translational Science Award Consortium, NCRR, NIH (grant UL1-TR-000117).
Publisher Copyright:
© 2016, American College of Rheumatology.
Financiación
Drs. Salt and Huaman's work was supported in part by the National Center for Research Resources (NCRR) and the National Center for Advancing Translational Sciences, NIH (grant UL1-TR-000117). Access to the large commercially insured data set was made available with funding from the Clinical and Translational Science Award Consortium, NCRR, NIH (grant UL1-TR-000117).
| Financiadores | Número del financiador |
|---|---|
| Clinical and Translational Science Award Consortium | |
| National Institutes of Health (NIH) | UL1-TR-000117 |
| National Center for Research Resources | |
| National Center for Advancing Translational Sciences (NCATS) | KL2TR000116 |
ODS de las Naciones Unidas
Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible
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Good health and well being
ASJC Scopus subject areas
- Immunology and Allergy
- Rheumatology
- Immunology
Huella
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