Inhaled Corticosteroid-Containing Treatment Escalation and Outcomes for Patients with Asthma in a U.S. Health Care Organization

Adult Male Dose-Response Relationship, Drug Middle Aged Patient Acceptance of Health Care Asthma United States 3. Good health Cohort Studies Insurance Claim Review Young Adult 03 medical and health sciences Treatment Outcome 0302 clinical medicine Adrenal Cortex Hormones Administration, Inhalation Humans Female Anti-Asthmatic Agents
DOI: 10.18553/jmcp.2017.23.11.1149 Publication Date: 2017-10-30T16:49:34Z
ABSTRACT
Asthma is a common disorder that affects approximately 8% of the U.S.Treatment guidelines indicate inhaled corticosteroids (ICS) as mainstay treatment, yet poor asthma control among ICS-treated patients. Treatment escalation (ICS dose increase and other controller therapy add-ons) used to manage symptoms. Real-world studies postescalation outcomes may inform treatment decisions.To (a) describe characteristics patterns patients who escalated (b) assess (exacerbations, uncontrolled asthma, health care resource utilization [HCRU]) after escalation.The study cohort was identified from large U.S. administrative claims database via ICD-9-CM codes for (493.xx on ≥ 2 dates) initiation (defining index date) long-term (> 1 fill) ICS-containing between January 1, 2009, September 30, 2014. One year continuous enrollment required before date. Escalation defined following: ICS increase; switch ICS, long-acting beta-2 agonists (LABA), or leukotriene modifiers (LTRM) different LABA, LTRM; add-on medications (e.g., antibody biologic). were examined. Rates exacerbation (defined by inpatient admission, emergency department [ED] visit, office visit with pharmacy claim an oral corticosteroid [OCS] within 7 days) occurrence > 4 fills short-acting beta agonist [SABA] in 1-year period, OCS fill, asthma-related ED admission) calculated. Per-patient-per-year (PPPY) HCRU estimated.Among 35,126 (mean [SD] age 38 [16] years) initiated 5,044 (14%) their regimens at 136 (105) days post-index (i.e., pre-escalation period). The most frequent changes, alone combination, included (68%) LABA (27%) LTRM (25%) add-ons. Before escalation, rate 1.60 (5.10) PPPY, 1,108 (22%) experienced exacerbation. During period 251.6 (138.9) days, 0.75 (2.9) 1,038 (21%) A majority 85%) exacerbations periods associated plus days. Uncontrolled 41.5% 41.0% respectively. Ambulatory visits 24.0 [26.7] all-cause 8.5 [13.4] PPPY) (19.3 [21.3] 4.6 [8.1] PPPY).Among regimen, 14% initiation. Yet, 21% those had exacerbation, 41% escalation. results demonstrate unmet need treatment.This sponsored funded Boehringer-Ingelheim, which contracted Optum conduct research. sponsor collaborated preparation, writing, revision, approval manuscript. Bengston, Cao, Hulbert, Wolbeck, Elliott, Buikema are employees Optum. Yu Wang employed Boehringer-Ingelheim. Study concept design contributed Yu, Wang. Wolbeck collected data, data analysis performed manuscript written along Wang, revised authors.
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