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Tirzepatide 2026-07-12 PubMed

Real-world tirzepatide users prioritize health, report high ease of use despite cost barriers

Understanding reasons for initiation and experience with tirzepatide among individuals with obesity or overweight: Results from the PERCEPTIONS survey.

Background

Despite the proven efficacy of tirzepatide in clinical trials like SURMOUNT for significant weight reduction and improved health-related quality of life (HRQoL) in individuals with obesity or overweight, there remains a critical gap in understanding real-world patient experiences. Specifically, the motivators and barriers to initiating tirzepatide, as well as the practical ease of use, have been underexplored outside of controlled trial settings. This real-world perspective is crucial for informing patient counseling, addressing access challenges, and optimizing adherence to obesity medication (OM) therapies.

Study Design

This descriptive, real-world, observational study, known as the PERCEPTIONS survey, collected baseline data from 518 adults in the US between June and November 2025. Participants were eligible for obesity medication, had obesity (BMI ≥30 kg/m2) or overweight (BMI ≥27 kg/m2 with ≥1 obesity-related complication), and did not have type 2 diabetes mellitus. The survey was completed within 4-8 weeks of the participants' first tirzepatide dose. Key questions focused on demographic and clinical characteristics, prior treatments, patient-reported outcomes, and, critically, motivators and barriers to treatment initiation, alongside the perceived ease of tirzepatide use.

Results

The study included 518 participants (mean age: 46.0 years, 78.2% female, mean BMI: 38.4 kg/m2). The average time between the first tirzepatide dose and survey completion was approximately ~26 days. A significant majority, 89.2%, initiated tirzepatide at the 2.5 mg dose, with 12.7% having previously used semaglutide. Nearly half of participants had struggled to achieve or maintain weight reduction through diet and exercise alone. Participants reported substantial impairments in physical functioning and psychosocial well-being at baseline, along with high internalized weight bias. Primary motivators for starting tirzepatide included improving overall health and well-being (83.8%), enhancing physical functioning (58.3%), and boosting self-confidence/appearance (51.4%). However, significant barriers were identified: concerns about treatment cost (57.7%) and health insurance coverage (90%).

Key Findings

  • Primary motivators for tirzepatide initiation were improving overall health (83.8%), physical functioning (58.3%), and self-confidence (51.4%).
  • Major barriers to tirzepatide initiation included concerns about treatment cost (57.7%) and health insurance coverage (90%).
  • The vast majority of users found tirzepatide easy to use (98.0% auto-injector, 95.8% vial users).
  • Most participants (89.2%) initiated tirzepatide at the 2.5 mg dose.
  • Participants reported significant impairments in physical functioning and psychosocial well-being at tirzepatide initiation.

Why It Matters

This real-world data provides valuable insights for both patients and healthcare providers, highlighting the patient-centric reasons for initiating tirzepatide beyond just weight loss. Prescribers can leverage these findings to better counsel patients, emphasizing the potential for improved overall health, physical function, and self-confidence as key motivators. The high reported ease of use (98.0% for auto-injector, 95.8% for vial users) suggests that the administration method is not a significant barrier to adherence, which is crucial for long-term success. However, the overwhelming concern about cost and insurance coverage (90%) underscores a critical access challenge that policy makers and payers must address to ensure equitable access to effective obesity treatments like tirzepatide.


tirzepatide obesity overweight patient experience real-world-evidence health-related-quality-of-life
Source: pubmed:42436850 · Ingested 2026-07-12 · Digest: gemini-2.5-flash