Characteristics of Users and New Initiators of Single- and Multiple-Inhaler Triple Therapy for Chronic Obstructive Pulmonary Disease in Germany

Int J Chron Obstruct Pulmon Dis. 2024 Apr 17:19:945-956. doi: 10.2147/COPD.S431291. eCollection 2024.

Abstract

Purpose: To assess patient characteristics of users and new initiators of triple therapy for chronic obstructive pulmonary disease (COPD) in Germany.

Patients and methods: Retrospective cohort study of patients with COPD and ≥1 prescription for single-inhaler triple therapy (SITT; fluticasone furoate/umeclidinium/vilanterol [FF/UMEC/VI] or beclomethasone dipropionate/glycopyrronium bromide/formoterol [BDP/GLY/FOR]) or multiple-inhaler triple therapy (MITT), using data from the AOK PLUS German sickness fund (1 January 2015-31 December 2019). The index date was the first date of prescription for FF/UMEC/VI or BDP/GLY/FOR (SITT users), or the first date of overlap of inhaled corticosteroid, long-acting β2-agonist, and long-acting muscarinic antagonist (MITT users). Two cohorts were defined: the prevalent cohort included all identified triple therapy users; the incident cohort included patients newly initiating triple therapy for the first time (no prior use of MITT or SITT in the last 2 years). Patient characteristics and treatment patterns were assessed on the index date and during the 24-month pre-index period.

Results: In total, 18,630 patients were identified as prevalent triple therapy users (MITT: 17,945; FF/UMEC/VI: 700; BDP/GLY/FOR: 908; non-mutually exclusive) and 2932 patients were identified as incident triple therapy initiators (MITT: 2246; FF/UMEC/VI: 311; BDP/GLY/FOR: 395; non-mutually exclusive). For both the prevalent and incident cohorts, more than two-thirds of patients experienced ≥1 moderate/severe exacerbation in the preceding 24 months; in both cohorts more BDP/GLY/FOR users experienced ≥1 moderate/severe exacerbation, compared with FF/UMEC/VI and MITT users. Overall, 97.9% of prevalent triple therapy users and 86.4% of incident triple therapy initiators received maintenance treatment in the 24-month pre-index period.

Conclusion: In a real-world setting in Germany, triple therapy was most frequently used after maintenance therapy in patients with recent exacerbations, in line with current treatment recommendations.

Keywords: COPD; Germany; MITT; SITT; patient characteristics; real-world treatment.

Plain language summary

Triple therapy (a combination of three different respiratory inhaled medications) is recommended for patients with chronic obstructive pulmonary disease (COPD) who experience repeated short-term symptom flare-ups when taking dual therapy (a combination of two different respiratory medications). Previously, patients had to take triple therapy using two or three separate inhalers. More recently, single-inhaler triple therapies have been developed, meaning patients can take all three different medications at the same time via one single inhaler. This study assessed the characteristics of patients who were already receiving triple therapy, or who started triple therapy (either via multiple inhalers or a single inhaler), in Germany between January 2015 and December 2019. In total, 18,630 patients who were already receiving triple therapy during the study period, and 2932 patients who newly started using triple therapy were included. The study reported that more than two-thirds of included patients had experienced at least one flare-up of COPD symptoms in the 2 years before starting triple therapy. Most patients had also received another therapy for COPD before starting triple therapy. A small proportion of patients started taking triple therapy after receiving no other therapy for COPD in the previous 2 years. The results of the study suggest that triple therapy for COPD in Germany is most often used in accordance with recommendations (patients already receiving therapy and experiencing repeated symptom flare-ups).

MeSH terms

  • Administration, Inhalation
  • Adrenergic beta-2 Receptor Agonists* / administration & dosage
  • Adrenergic beta-2 Receptor Agonists* / adverse effects
  • Aged
  • Aged, 80 and over
  • Beclomethasone / administration & dosage
  • Beclomethasone / adverse effects
  • Benzyl Alcohols / administration & dosage
  • Benzyl Alcohols / adverse effects
  • Bronchodilator Agents* / administration & dosage
  • Bronchodilator Agents* / adverse effects
  • Chlorobenzenes / administration & dosage
  • Chlorobenzenes / adverse effects
  • Drug Combinations*
  • Drug Therapy, Combination
  • Female
  • Formoterol Fumarate / administration & dosage
  • Germany
  • Glycopyrrolate* / administration & dosage
  • Glycopyrrolate* / adverse effects
  • Humans
  • Male
  • Middle Aged
  • Muscarinic Antagonists* / administration & dosage
  • Muscarinic Antagonists* / adverse effects
  • Nebulizers and Vaporizers*
  • Pulmonary Disease, Chronic Obstructive* / diagnosis
  • Pulmonary Disease, Chronic Obstructive* / drug therapy
  • Pulmonary Disease, Chronic Obstructive* / physiopathology
  • Quinuclidines / administration & dosage
  • Quinuclidines / adverse effects
  • Retrospective Studies
  • Time Factors
  • Treatment Outcome

Substances

  • Muscarinic Antagonists
  • Bronchodilator Agents
  • Adrenergic beta-2 Receptor Agonists
  • Glycopyrrolate
  • Drug Combinations
  • GSK573719
  • Chlorobenzenes
  • Quinuclidines
  • Benzyl Alcohols
  • Beclomethasone
  • Formoterol Fumarate

Grants and funding

This study was funded by GSK (study number 214666). GSK-affiliated authors were involved in study conception and design, data analysis, data interpretation, and the decision to submit the article for publication. GSK funded the article processing charges and Open Access fee.