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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
被引:3
|作者:
Kingsberg, Sheryl
[1
]
Banks, Victoria
[2
]
Caetano, Cecilia
[3
]
Janssenswillen, Cecile
[3
]
Moeller, Carsten
[4
]
Schoof, Nils
[4
]
Harvey, Mia
[5
]
Scott, Megan
[5
]
Nappi, Rossella E.
[6
,7
]
机构:
[1] Case Western Reserve Univ, Univ Hosp Cleveland Med Ctr, Sch Med, Cleveland, OH 44106 USA
[2] Bayer, Reading, England
[3] Bayer Consumer Care, Basel, Switzerland
[4] Bayer AG, Berlin, Germany
[5] Adelphi Real World, Bollington, England
[6] Univ Pavia, Dept Clin Surg Diagnost & Pediat Sci, Pavia, Italy
[7] IRCCS San Matteo Fdn, Res Ctr Reprod Med, Gynecol Endocrinol & Menopause Obstet & Gynecol Un, Pavia, Italy
来源:
关键词:
Menopause;
Vasomotor symptoms (VMS);
Sleep;
Depression;
Complementary alternative medicine (CAM);
Drug utilization;
QUALITY-OF-LIFE;
ALTERNATIVE MEDICINE;
HORMONE-THERAPY;
PREVALENCE;
MANAGEMENT;
COMPLEMENTARY;
KNOWLEDGE;
IMPACT;
SLEEP;
D O I:
10.1016/j.maturitas.2024.108096
中图分类号:
R592 [老年病学];
C [社会科学总论];
学科分类号:
03 ;
0303 ;
100203 ;
摘要:
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 ProgrammeTM, 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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