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Real-world evaluation of treatment utilization by women experiencing vasomotor symptoms associated with menopause in the United States and Europe: Findings from the REALISE study.
Kingsberg, Sheryl; Banks, Victoria; Caetano, Cecilia; Janssenswillen, Cecile; Moeller, Carsten; Schoof, Nils; Harvey, Mia; Scott, Megan; Nappi, Rossella E.
Afiliação
  • Kingsberg S; University Hospitals Cleveland Medical Center, Case Western Reserve University School of Medicine, United States. Electronic address: Sheryl.Kingsberg@UHhospitals.org.
  • Banks V; Bayer, Reading, United Kingdom.
  • Caetano C; Bayer Consumer Care, Basel, Switzerland.
  • Janssenswillen C; Bayer Consumer Care, Basel, Switzerland.
  • Moeller C; Bayer AG, Berlin, Germany.
  • Schoof N; Bayer AG, Berlin, Germany.
  • Harvey M; Adelphi Real World, Bollington, United Kingdom.
  • Scott M; Adelphi Real World, Bollington, United Kingdom.
  • Nappi RE; Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, Pavia, Italy; Research Center for Reproductive Medicine, Gynecological Endocrinology and Menopause, Obstetrics and Gynecology Unit, IRCCS San Matteo Foundation, Pavia, Italy.
Maturitas ; 189: 108096, 2024 Aug 22.
Article em En | MEDLINE | ID: mdl-39208496
ABSTRACT

OBJECTIVES:

Despite the profound impact of menopausal symptoms on women, treatment utilization is low, and many seek alternative therapies. The REALISE study aimed to evaluate the treatment landscape - that is, pharmacological treatment, lifestyle changes (LC), and use of over-the-counter (OTC) products - for women from six high-income countries experiencing vasomotor symptoms (VMS) and receiving healthcare. STUDY

DESIGN:

Analysis of a secondary dataset, the Adelphi Real World Disease Specific Programme™, a large, cross-sectional, point-in-time survey conducted in the United States and five European countries (February-October 2020). Physicians provided demographic, clinical, and treatment data; women were stratified by VMS severity (mild; moderate-severe) and presence of concomitant sleep/mood symptoms. Women completed forms on VMS severity, concomitant symptoms, LC, and OTC product use. Two subgroups were identified VMS-only and VMS + sleep/mood. MAIN OUTCOME

MEASURES:

Prescription treatment, LC, and OTC product utilization.

RESULTS:

Physicians (n = 233) provided data on 1767 women; 825 (46.7 %) completed a self-completion form. Physicians rated 60 % of women with moderate-severe VMS, of whom 709 (66.8 %) were currently prescribed pharmacological treatment; 27.1 % had never been prescribed. Hormone therapy was most frequently prescribed in the moderate-severe group (overall, 49.8 %; VMS-only, 57.4 %; VMS + sleep/mood, 47.3 %), followed by serotonergic antidepressants (15.7 %; 9.7 %; 17.6 %, respectively). Most women (78.3 %) with moderate-severe VMS adopted LC, and 57.6 % used at least one OTC product for VMS relief.

CONCLUSIONS:

Nearly a third of women with moderate-severe VMS had never received treatment despite access to healthcare. This, combined with the prevalent use of LC/OTC products, suggests an unmet need for new treatment options to manage VMS and concomitant sleep/mood symptoms.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Maturitas Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Maturitas Ano de publicação: 2024 Tipo de documento: Article