Rhinitis, sinusitis, and upper airway disease
Incidence and associated premorbid diagnoses of patients with chronic rhinosinusitis

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Background

Chronic rhinosinusitis (CRS) is a prevalent condition with underexplored risk factors.

Objectives

We sought to determine CRS incidence and evaluate associations with a range of premorbid medical conditions for chronic rhinosinusitis without nasal polyps (CRSsNP) and chronic rhinosinusitis with nasal polyps (CRSwNP) using real-world clinical practice data.

Methods

Electronic health records data from 446,480 Geisinger Clinic primary care patients were used for a retrospective longitudinal cohort study for data from 2001-2010. By using logistic regression, newly diagnosed CRS cases between 2007 and 2009 were compared with frequency-matched control subjects on premorbid factors in the immediate (0-6 months), intermediate (7-24 months), and entire observed timeframes before diagnosis.

Results

The average incidence of CRS was 83 ± 13 CRSwNP cases per 100,000 person-years and 1048 ± 78 CRSsNP cases per 100,000 person-years. Between 2007 and 2009, 595 patients with incident CRSwNP and 7523 patients with incident CRSsNP were identified and compared with 8118 control subjects. Compared with control subjects and patients with CRSsNP, patients with CRSwNP were older and more likely to be male. Before diagnosis, patients with CRS had a higher prevalence of acute rhinosinusitis, allergic rhinitis, chronic rhinitis, asthma, gastroesophageal reflux disease, adenotonsillitis, sleep apnea, anxiety, and headaches (all P < .001). Patients with CRSsNP had a higher premorbid prevalence of infections of the upper and lower airway, skin/soft tissue, and urinary tract (all P < .001). In the immediate and intermediate timeframes analyzed, patients with CRS had more outpatient encounters and antibiotic prescriptions (P < .001), but guideline-recommended diagnostic testing was performed in a minority of cases.

Conclusions

Patients who are given a diagnosis of CRS have a higher premorbid prevalence of anxiety, headaches, gastroesophageal reflux disease, sleep apnea, and infections of the respiratory system and some nonrespiratory sites, which results in higher antibiotic, corticosteroid, and health care use. The use of guideline-recommended diagnostic testing for confirmation of CRS remains poor.

Section snippets

Study overview

We used longitudinal data from the EHRs of patients with a Geisinger Clinic primary care provider to first calculate annual incidence rates from 2001-2009 and then complete a nested case-control analysis. The goals were as follows: (1) describe the epidemiology of CRS; (2) compare the prevalence and timing of premorbid illnesses preceding incident CRSwNP and CRSsNP compared with those in control subjects; (3) compare health care and antibiotic use among patients with CRSwNP and CRSsNP compared

Description of study population and annual incidence

Data on 307,381 patients who received care at any time in the years 2007, 2008, and 2009 were analyzed to identify 595 incident CRSwNP cases, 7523 incident CRSsNP cases, and 8118 matched control subjects (Table I). The average incidence rate from 2007-2009 was 83 ± 13 CRSwNP cases per 100,000 person-years and 1048 ± 78 CRSsNP cases per 100,000 person-years. Comparing the study time period 2007-2009 with 2001-2006, the incidence of CRSsNP was stable, whereas the incidence of CRSwNP appeared to

Discussion

In this study we used 10 years of data from a large cohort of primary care patients from the EHRs of the dominant health care provider serving an expansive geographic region to evaluate the epidemiology of CRS, test several previously proposed hypotheses regarding the pathobiology of CRS, and examine how CRS is being treated and diagnosed in the community. To our knowledge, this study has provided the first estimate of the incidence of physician-diagnosed CRS. Our study shows a remarkable

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    Supported by National Institutes of Health grants K23DC012067 (to B.K.T.), R01 HL068546, R01 HL078860, and R01 AI072570, as well as the Ernest S. Bazley Trust (to R.P.S.).

    Disclosure of potential conflict of interest: B. K. Tan has been supported by one or more grants from the National Institutes of Health (NIH), has received one or more grants from or has one or more grants pending with the Triological Society, and has received one or more payments for travel/accommodations/meeting expenses from the Foundation for Innovation, Education, and Research in Otorhinolaryngology. J. Pollak is employed by Johns Hopkins Bloomberg School of Public Health. A. T. Peters has provided expert testimony regarding Stevens-Johnson syndrome and has received one or more payments for lecturing from or is on the speakers' bureau for Baxter. R. P. Schleimer has been supported by one or more grants from the NIH and has consultancy arrangements with Intersect ENT, GlaxoSmithKline, and Allakos. B. S. Schwartz has been supported by one or more grants from Northwestern University. The rest of the authors declare that they have no relevant conflicts of interest.

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