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International Urogynecology Journal

, Volume 30, Issue 2, pp 251–256 | Cite as

Increased risk for stress urinary incontinence in women with postmenopausal hormone therapy

  • Päivi Rahkola-Soisalo
  • Hanna Savolainen-Peltonen
  • Mika Gissler
  • Fabian Hoti
  • Pia Vattulainen
  • Olavi Ylikorkala
  • Tomi S. MikkolaEmail author
Original Article

Abstract

Introduction and hypothesis

The impact of estradiol-based hormone therapy (HT) on the incidence of stress urinary incontinence (SUI) is unknown. Therefore, we compared the use of such HT regimens and tibolone in women with and without SUI.

Methods

The women with a history of SUI operation (N = 15,002) were identified from the Finnish National Hospital Discharge Register, and the control women without such an operation (N = 44,389) from the Finnish Central Population Register. The use of HT was traced from the National Drug Reimbursement Register, and the odd ratios (ORs) with 95% confidence intervals (95% CIs) for SUI were calculated by using the conditional logistic regression analysis.

Results

The cases had used any HT more often than the controls. The use of systemic estradiol-only or estradiol–progestin therapy was accompanied by an increased SUI risk (OR 3.8, 95% CI: 3.6–4.0 and OR 2.7, 95% CI: 2.6–2.9 respectively). The use of estradiol with noretisterone acetate showed a higher risk of increase than that with medroxyprogesterone acetate. Age over 55 years at the initiation of systemic HT was accompanied by a higher SUI risk increase than that under 55 years of age. The use of tibolone, an estradiol + levonorgestrel-releasing intrauterine device, or vaginal estradiol also increased the risk.

Conclusions

The use of HT regimens may predispose to the de novo development or worsening of pre-existing SUI. Thus, caution is needed when these regimens are prescribed to women with mild stress-related urine leakage or with established SUI risk factors.

Keywords

Estradiol Hormone therapy Menopause Stress urinary incontinence 

Notes

Compliance with ethical standards

Conflicts of interest

PR-S has received funding for congress attendance from Johnson & Johnson and Astellas Pharma. HS-P has been a speaker for Mylan and received funding for congress attendance from Mylan and MSD. TM has been a speaker and/or received consulting fees from Mylan and Astellas Pharma.

MG and OY have nothing to disclose. FH and PV work for EPID Research. EPID Research is a company that performs financially supported studies for several pharmaceutical companies.

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Copyright information

© The International Urogynecological Association 2018

Authors and Affiliations

  • Päivi Rahkola-Soisalo
    • 1
  • Hanna Savolainen-Peltonen
    • 1
    • 2
  • Mika Gissler
    • 3
    • 4
  • Fabian Hoti
    • 5
  • Pia Vattulainen
    • 5
  • Olavi Ylikorkala
    • 1
  • Tomi S. Mikkola
    • 1
    • 2
    Email author
  1. 1.Department of Obstetrics and GynecologyUniversity of Helsinki and Helsinki University HospitalHelsinkiFinland
  2. 2.Folkhälsan Research CenterBiomedicumHelsinkiFinland
  3. 3.National Institute for Health and WelfareHelsinkiFinland
  4. 4.Department of Neurobiology, Care Sciences and Society, Division of Family MedicineKarolinska InstitutetStockholmSweden
  5. 5.EPID Research OyEspooFinland

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