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The cost of simplifying treatments for cystic fibrosis: Implications of the SIMPLIFY trial.
Gold, Laura S; Hansen, Ryan N; Mayer-Hamblett, Nicole; Nichols, David P; Gifford, Alex H; Kloster, Margaret; Goss, Christopher H; Kessler, Larry.
Afiliação
  • Gold LS; Department of Radiology, University of Washington, Seattle.
  • Hansen RN; School of Pharmacy, University of Washington, Seattle.
  • Mayer-Hamblett N; Department of Health Systems and Population Health, University of Washington, Seattle.
  • Nichols DP; Seattle Children's Research Institute, WA.
  • Gifford AH; Department of Biostatistics, University of Washington, Seattle.
  • Kloster M; Department of Pediatrics, University of Washington, Seattle.
  • Goss CH; Department of Pediatrics, University of Washington, Seattle.
  • Kessler L; Department of Medicine, Case Western Reserve University, Cleveland, OH.
J Manag Care Spec Pharm ; 30(1): 26-33, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38153868
ABSTRACT

BACKGROUND:

Dornase alfa and hypertonic saline are mucoactive therapies that can improve respiratory symptoms in people with cystic fibrosis (CF). A recent randomized control trial showed that participants with well-preserved pulmonary function taking elexacaftor + tezacaftor + ivacaftor (ETI) who discontinued dornase alfa or hypertonic saline for 6 weeks had no clinically meaningful decline in lung function. This may prompt discussions with care providers regarding ongoing use of these medications.

OBJECTIVE:

To compare the costs of outpatient medications between people taking ETI who continued or discontinued (1) dornase alfa or (2) hypertonic saline from 2 clinical trials and project cost differences in the US CF population if these 2 medications were used only intermittently for symptom relief instead of chronically.

METHODS:

The SIMPLIFY study was 2 parallel multicenter trials that randomized participants 11 to either continue or discontinue therapy. To estimate costs, we used data from the Merative MarketScan Databases to identify people with CF from 2020 to 2021. Our primary outcomes were differences in costs of outpatient prescription drugs among those who continued vs discontinued dornase alfa and, separately, hypertonic saline. We obtained adjusted differences in median costs. To estimate the annual cost savings if the population of people with CF taking ETI used these medications only intermittently, we multiplied the proportion of people in MarketScan with CF diagnoses who were taking each of these medications by the median cost savings per year and subtracted the cost of "rescue" use.

RESULTS:

A total of 392 participants from the dornase alfa trial and 273 from the hypertonic saline trial were included in analyses. The adjusted difference in median medication costs was not significant for the hypertonic saline trial, but we observed a significantly decreased 6-week cost of medications in the dornase alfa trial (adjusted median difference in costs between discontinue and continue of $5,860 (95% CI = $4,870-$6,850); P < 0.0001). We estimated that two-thirds of people with CF use ETI and dornase alfa in the United States; if they discontinued dornase alfa except for intermittent use, the resulting annual savings would be $1.21 billion.

CONCLUSIONS:

Although the costs of dornase alfa and hypertonic saline are smaller compared with ETI, reduction in use would lead to substantial prescription drug cost savings and reduce the treatment burden. However, individual benefits of these therapies should be considered, and decisions regarding changes in therapy remain an important discussion between people with CF and their providers. Study registration number NCT04378153.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrose Cística / Medicamentos sob Prescrição Limite: Humans Idioma: En Revista: J Manag Care Spec Pharm Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrose Cística / Medicamentos sob Prescrição Limite: Humans Idioma: En Revista: J Manag Care Spec Pharm Ano de publicação: 2024 Tipo de documento: Article