Review question
What are the effects of pelvic floor muscle training (PFMT) given in combination with other treatments to women with urinary incontinence?
Relevance to primary care and nursing
Urinary incontinence is a common problem in women who report a wide range of urinary symptoms, which progress with age and significantly affect the overall quality of life (QoL). Estimated prevalence rates range from 30 to 60% in middle-aged and older women and rise with advancing age. Although a number of conservative, pharmacological and surgical treatment options are available, the financial impact of the condition is substantial. Primary health-care nurses and doctors have a key role in the management of urinary incontinence in women (National Institute for Health and Clinical Excellence, 2013) and this systematic review aimed to determine the effectiveness of adding PFMT to any of the other active treatments.
Characteristics of the evidence
This Cochrane review contained 11 randomised controlled trials targeting adult women with clinical or urodynamic evidence of stress urinary incontinence (SUI), urgency urinary incontinence (UUI) or mixed urinary incontinence (MUI) (Ayeleke et al., Reference Ayeleke, Hay-Smith and Omar2013).
Included trials compared PFMT added to another active treatment (n=494) with the same active treatment alone (n=490). PFMT was defined as a programme of repeated voluntary pelvic floor muscle contractions taught and/or supervised by health-care professionals. PFMT programmes varied considerably; common variations included number and frequency of contractions, use of biofeedback and number of health professional contacts. PFME programmes were also commonly accompanied by advice on managing urgency and frequency, and lifestyles advice (e.g., weight reduction). PFMT programmes ranged from 4 to 12 weeks long, and addressed muscle strength, endurance, coordination or a combination of these (although in six trials insufficient description made the exercise difficult to characterise). Active comparators included vaginal cones, bladder training, electrical stimulation, continence pessary, various drug therapies and others such as heat and steam generating sheets. The interventions were delivered by nurses, physical therapists and/or doctors.
Exclusions: studies of antenatal or postnatal women, or women whose symptoms were complicated by other co-morbidities (e.g., cognitive impairment, neurological conditions, frailty).
Summary of key evidence
Most included trials were assessed as unclear risk of bias for most of the methodological domains, and the overall quality of evidence was rated as low. Moreover, most of the included trials did not report outcomes that were important from patients’ perspective. Meta-analysis was not possible as most comparisons were reported by single trials and outcomes. The total number of participants and effect sizes, means and risk ratio (RR), 95% confidence intervals (CI) are shown in parentheses where appropriate. The findings are summarised according to types of interventions.
Primary outcomes: number of women reporting ‘cured’ (100% reduction) or ‘improved’ (⩾50% reduction) in incontinence; condition-specific QoL; patient global impression of improvement.
Secondary outcomes: frequency of incontinence episodes; objective assessment of improvement; number of continence pads used; frequency of micturition; volume of urine per micturition.
Other outcomes: patient satisfaction with treatment outcome.
Physical interventions
PFMT added to vaginal cones versus vaginal cones alone: one trial of women with SUI (n=42) showed no significant effect on women cured or improved (objective assessment) with SUI at 12 weeks.
Behavioural interventions
PFMT added to bladder training versus bladder training alone in women with SUI, UUI or MUI: one trial (n=135), reported a cure or an improvement in incontinence and QoL immediately after treatment, but not at three months. There was a non-significant reduction in the frequency of incontinence episodes, and no differences in the number of women who relapsed from three months to three years follow-up.
Electrical/magnetic interventions
PFMT added to electrical stimulation versus electrical stimulation alone (excluding implanted electrodes): one small trial (n=22) showed no significant effect of the intervention on cure or improvement in women with SUI at six weeks. Effect size in one small study examining magnetic stimulation was not estimable.
Mechanical interventions
PFMT added to continence pessaries versus continence pessaries alone: evidence from one trial (n=299) showed no significant effect on cure or improvement, QoL or on patient global impression of improvement or patient satisfaction at 3, 6 or 12 months in women with SUI.
Drug interventions with and without PFMT
Each drug was tested only in single trials. PFMT added to duloxetine (n=104), oxybutynin (n=64), solifenacin (n=162) and clenbutarol (n=41) showed no significant effect on any reported outcomes. Only one small trial (n=29) testing an unspecified drug therapy showed that significantly more women reported benefit from combined treatment (RR 2.57, 95% CI 1.06–6.20).
Other interventions
PFMT plus heat and steam generating sheet versus heat and steam generating sheet alone: only one trial (n=74) of women with UUI or MUI showed a significant effect of the combined intervention on number of women cured (RR 2.38, 95% CI 1.19–4.73).
Implications for practice
Most evidence came from small under-powered trials, making it difficult to draw conclusions from insufficient evidence on effectiveness or efficacy of PFMT, as most included trials did not examine adverse events associated with PFMT.
Implications for research
The overall quality of evidence was low and high-quality research is required to evaluate the effect of adjunctive PFMT for urinary incontinence in women. None of the trials investigated PFMT with and without surgical intervention or lifestyle interventions, which warrant further investigations. There is a need to focus on QoL, socio-economic implications, long-term effects and adverse events associated with combining PFMT with other active treatments.
Acknowledgement
The author is a member of the Cochrane Nursing Care Field (CNCF).
Financial Support
This research received no specific grant from any funding agency, commercial or not-for-profit sectors.
Conflicts of Interest
None.