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Игольная суспензия шейки мочевого пузыря для лечения недержания мочи у женщин

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Abstract

Background

Bladder neck needle suspension is an operation traditionally used for moderate or severe stress urinary incontinence in women. About a third of adult women experience some urinary incontinence, and about a third of these have moderate or severe symptoms.

Objectives

To determine the effects of needle suspension on stress or mixed urinary incontinence in comparison with other management options.

Search methods

We searched the Cochrane Incontinence Group Specialised Register, which contains trials identified from the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, MEDLINE in process, ClinicalTrials.gov, WHO ICTRP and handsearching of journals and conference proceedings (searched 12 November 2014), and the reference lists of relevant articles.

Selection criteria

Randomised or quasi‐randomised trials that included needle suspension for the treatment of urinary incontinence.

Data collection and analysis

At least two authors assessed trials and extracted data independently. Two trial investigators provided additional information.

Main results

We identified 10 trials, which included 375 women having six different types of needle suspension procedures and 489 who received comparison interventions. Needle suspensions were more likely to fail than open abdominal retropubic suspension. There was a higher subjective failure rate after the first year (91/313 (29%) failed versus 47/297 (16%) failed after open abdominal retropubic suspension). The risk ratio (RR) was 2.00 (95% confidence interval (CI) 1.47 to 2.72), although the difference in peri‐operative complications was not significant (17/75 (23%) versus 12/77 (16%); RR 1.44, 95% CI 0.73 to 2.83). There were no significant differences for the other outcome measures. This effect was seen in both women with primary incontinence and women with recurrent incontinence after failed primary operations. Needle suspensions may be as effective as anterior vaginal repair (50/156 (32%) failed after needle suspension versus 64/181 (35%) after anterior repair; RR 0.86, 95% CI 0.64 to 1.16), but there was little information about morbidity. Data for comparison with suburethral slings were inconclusive because they came from a small and atypical population.

No trials compared needle suspensions with conservative management, peri‐urethral injections, or sham or laparoscopic surgery.

Authors' conclusions

Bladder neck needle suspension surgery is probably not as good as open abdominal retropubic suspension for the treatment of primary and secondary urodynamic stress incontinence because the cure rates were lower in the trials reviewed. However, the reliability of the evidence was limited by poor quality and small trials. There was not enough information to comment on comparisons with suburethral sling operations. Although cure rates were similar after needle suspension compared with after anterior vaginal repair, the data were insufficient to be reliable and inadequate to compare morbidity.

PICOs

Population
Intervention
Comparison
Outcome

The PICO model is widely used and taught in evidence-based health care as a strategy for formulating questions and search strategies and for characterizing clinical studies or meta-analyses. PICO stands for four different potential components of a clinical question: Patient, Population or Problem; Intervention; Comparison; Outcome.

See more on using PICO in the Cochrane Handbook.

Резюме на простом языке

Хирургическая коррекция методом игольной суспензии при недержании мочи у женщин

Актуальность

Стрессовое недержание мочи ‐ это непроизвольное выделение мочи при кашле, смехе, чихании или физических упражнениях. К недержанию мочи могут привести нарушения со стороны мышц, поддерживающих мочевой пузырь. У около трети взрослых женщин может быть вытекание мочи и у трети из них могут быть проблемы, требующие хирургического вмешательства.

Когда нехирургические методы, такие как упражнения для мышц тазового дна (нижнее основание живота) или лекарственная терапия не эффективны, иногда прибегают к хирургическому вмешательству для поднятия и поддержки шейки мочевого пузыря, что способствует прекращению вытекания мочи. Хирургический метод игольной/игольчатой суспензии представляет собой наложение швов между влагалищем и брюшной стенкой.

Характеристика исследований

В обзор были включены 10 клинических испытаний с участием 375 женщин, у которых применяли шесть различных видов операций методом игольной суспензии, в сравнении с 489 женщинами, которые получали другое лечение. Большинство клинических испытаний были небольшими или плохого качества, что делает результаты этого обзора менее надежными.

Основные результаты

Большее число женщин вылечилось после абдоминальных операций, таких как кольпосуспензия (84%), чем после игольной суспензии (71%): независимо от того, были у них предыдущие операции по поводу недержания мочи или нет. Было недостаточно доказательств в отношении осложнений, или в отношении того, как игольную суспензию сравнивали с другими видами операций. Операции с использованием техники игольной суспензии не сравнивали с консервативным лечением, таким как упражнения для мышц тазового дна, или медикаментозным лечением. Таким образом, игольная суспензия представляется менее эффективным методом лечения недержания мочи, чем абдоминальные хирургические методы, и нет достаточных доказательств для сравнения ее с другими способами лечения.

Authors' conclusions

Implications for practice

The limited evidence indicates that bladder neck needle suspension operations are worse than the open abdominal approach (retropubic suspension) for the treatment of primary or secondary urodynamic stress incontinence. However, data were inadequate for comparing morbidity. Although cure rates appeared to be similar after needle suspension when compared with anterior vaginal repair, the data were insufficient to be reliable. Comparison with suburethral sling operations was inconclusive because of the small and atypical population studied. There were no trials that compared needle suspension with conservative or other physical therapy or with self fixing slings or with laparoscopic retropubic suspensions or with peri‐urethral injections.

Postoperative surgical morbidity was poorly reported, and quality of life measures and economic outcomes inadequately reported, therefore the alternative treatments could not be compared in other ways. In treating benign disease, morbidity must be balanced against the chance of cure or improvement in quality of life, and the cost‐effectiveness of the options should also be considered.

Implications for research

Future research in incontinence should incorporate standardised, validated, preferably objective and simple outcome measures that are relevant to women who have incontinence, in order to allow comparison between studies. In particular, long‐term morbidity, quality of life, and psychological and economic outcomes should be incorporated.

Surgical trials related to stress incontinence should systematically address surgical morbidity outcomes such as adverse peri‐operative events, length of hospital stay, time to return to normal activities, de novo development of urge symptoms or detrusor overactivity, and especially the need for repeat surgery or alternative interventions. Long‐term follow‐up (at least one year, preferably five years or more) is essential for the proper evaluation of incontinence treatments.

Background

This is one of a series of inter‐related Cochrane reviews of surgical approaches to the management of urinary incontinence: anterior vaginal repair (Glazener 2001); suburethral slings (Rehman 2011); laparoscopic retropubic suspension (Dean 2006); open abdominal retropubic suspension (Lapitan 2012); peri‐urethral injections (Kirchin 2012); and artificial sphincters. The reader is referred to one review in this series for a background description of urinary incontinence in women, the principal categories of incontinence and the broad approaches to management (Glazener 2001). As well as surgery, these include medical (drug) and conservative (physical) approaches.

Surgical procedures to remedy urinary incontinence generally aim to lift and support the urethrovesical junction between the urethra and the bladder in order to increase bladder outlet resistance. There is disagreement, however, regarding the precise mechanism by which continence is achieved after surgery. The choice of procedures is often influenced by co‐existent problems, a surgeon's specialty and preference, and the physical features of the person affected. Numerous surgical methods have been described, but essentially they fall into seven categories:

  • open abdominal retropubic suspension (e.g. Burch colposuspension, Marshall‐Marchetti‐Krantz);

  • laparoscopic retropubic suspension;

  • anterior vaginal repair (anterior colporrhaphy) (e.g. Pacey, Kelly);

  • suburethral sling procedures;

  • bladder neck needle suspensions (e.g. Pereyra, Stamey, Raz);

  • peri‐urethral injections;

  • artificial sphincters.

This review concentrated on needle suspensions of the bladder neck (referred to as 'needle suspension' in this review).

Needle suspension may be performed from a vaginal or abdominal approach. A long needle is used to thread sutures from the vagina to the anterior abdominal fascia. The sutures are looped through to the para‐urethral tissue on each side of the bladder neck, thereby supporting it. There are three principal types (Pereyra, Stamey, Raz) and several modifications of each, such as site of initial approach (abdominal or vaginal), type of suture, site of attachment of the sutures, and the use of silastic spacers or Dacron sheaths to protect the suture from cutting through (Downs 1996). Cystoscopy (endoscopy), during or after the placement of the sutures, is used to check that the bladder has not been injured. The salient features are that the passage of the needle through the retropubic space is done blindly, and the support to the urethra is derived indirectly from the vaginal walls rather than directly to the urethra.

The wide variety of surgical treatments for urinary incontinence indicates the lack of consensus as to which procedure is the best. Guidelines using the available literature have been published, but were based on studies of mixed quality and type (Black 1996; Downs 1996; Fantl 1996; Jarvis 1994; Leach 1997). Provided that a sufficient number of adequate quality have been conducted, the most reliable evidence is likely to come from consideration of all well‐designed randomised controlled trials. Hence, there is a need for an easily accessible, periodically updated, comprehensive systematic review of such studies, which will not only help to identify optimal practice, but also highlight gaps in the evidence base.

Objectives

To determine the effects of needle suspension on stress or mixed urinary incontinence in comparison with other management options.

Methods

Criteria for considering studies for this review

Types of studies

All randomised or quasi‐randomised trials studying the effects of treatment for stress or mixed urinary incontinence in women, in which at least one management arm involved bladder neck needle suspension.

Types of participants

Adult women with urinary incontinence, diagnosed as having:

  • urodynamic stress incontinence (USI, urodynamic diagnosis of stress incontinence in the absence of detrusor contractions); or

  • stress urinary incontinence (SUI, clinical diagnosis); or

  • mixed incontinence (MUI, any stress incontinence plus other urinary symptoms such as: detrusor overactivity (urodynamic diagnosis); urge incontinence (clinical diagnosis); other types of incontinence; urgency; or frequency.

We accepted the classification of diagnoses as defined by the trialists.

Types of interventions

At least one arm of a trial must have involved needle suspension to treat urinary incontinence.

We made the following comparisons:

  1. Needle suspension compared with no treatment or sham operation.

  2. Needle suspension compared with conservative interventions (e.g. pelvic floor muscle training, electrical stimulation, cones, biofeedback).

  3. Needle suspension compared with open abdominal retropubic suspension (abdominal surgery).

  4. Needle suspension compared with suburethral sling procedures (abdominal and vaginal surgery).

  5. Needle suspension compared with anterior vaginal repair (anterior colporrhaphy, vaginal surgery).

  6. Needle suspension compared with laparoscopic retropubic suspension.

  7. Needle suspension compared with peri‐urethral injections.

  8. Needle suspension compared with drug treatment (e.g. adrenergic agonists).

  9. One method of needle suspension compared with another.

  10. One suture type compared with another for carrying out needle suspension operations.

Types of outcome measures

We selected the outcome measures used in this review on the basis of their relevance to the subjective cure or improvement of incontinence. We regard the principal measures of effectiveness as the proportion of women cured (continent or dry) following surgery, and the proportion of women whose symptoms are improved.

We adopted the recommendations made by the Standardisation Committee of the International Continence Society for outcomes of research investigating the effect of therapeutic interventions for women with urinary incontinence. These outcome categories include: women's observations (symptoms), quantification of symptoms, the clinician's observations (anatomical and functional), quality of life and socioeconomic measures (Lose 1998).

Relevant data could come from both history and questionnaire assessment, supplemented by the use of urinary diaries (including time and type of incontinence, frequency of micturition and voided volumes) and pad tests (quantitative estimate of weight of urine lost under standard conditions). This review also included other surgical information and adverse events as outcome measures.

A. Women's observations

  • Perception of cure and improvement in the short term (< 12 months) and longer term (> 12 months) (expressed as failure to cure or improve)

  • Urge symptoms or urge incontinence (clinical diagnosis without urodynamics)

B. Quantification of symptoms

  • Pad changes over 24 hours (from self reported number of pads used)

  • Incontinent episodes over 24 hours (from self completed bladder chart)

  • Pad tests of quantified leakage (mean volume or weight of urine loss)

C. Clinician's observations

  • Objective assessment of incontinence at urodynamics

  • Detrusor overactivity (urodynamic diagnosis)

  • New or recurrent prolapse

D. Quality of life

  • General health status measures (physical, psychological, other)

  • Condition‐specific health measures (specific instruments designed to assess incontinence)

E. Socioeconomic measures

  • Health economic measures

F. Surgical outcome measures

  • Voiding dysfunction/difficulty after three months (with or without urodynamic confirmation)

  • Peri‐operative surgical complications (e.g. vascular or visceral injury, haemorrhage, infection, bacteriuria, death associated with surgery)

  • Length of inpatient stay

  • Time to return to normal activity level

  • Dyspareunia (pain with intercourse)

  • Repeat incontinence surgery

  • Later prolapse surgery

  • Death

G. Other outcomes

  • Non‐prespecified outcomes judged important when performing the review

Search methods for identification of studies

We did not impose any language or other limits on the searches, details of which are given below.

Electronic searches

This review has drawn on the search strategy developed for the Cochrane Incontinence Review Group. We identified relevant trials from the Group's Specialised Register of controlled trials, which is described, along with the group search strategy, under the Incontinence Group's module in The Cochrane Library. The Register contains trials identified from the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, MEDLINE in process, ClinicalTrials.gov, the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP) and handsearching of journals and conference proceedings. We searched the Incontinence Group Specialised Register using the Group's own keyword system. The search terms used were:

({design.cct*} OR {design.rct*})
AND
({intvent.surg.bladnecsusp.*} OR {intvent.surg.needle.*})

(All searches were of the keyword field of Reference Manager 2012).

The date of the most recent search of the Register for this review was 12 November 2014.

Most of the trials in the Incontinence Group Specialised Register are also contained in CENTRAL.

Searching other resources

We searched the reference lists of relevant articles.

Data collection and analysis

Selection of studies

We identified randomised and quasi‐randomised trials using the above search strategy. We excluded studies if they were not randomised or quasi‐randomised trials for incontinent women. Excluded studies are listed with reasons for their exclusion. We resolved any differences of opinion related to study inclusion, methodological quality or data extraction by discussion with a third party.

Quality of trials

The review authors evaluated the reports of all possibly eligible trials for methodological quality and appropriateness for inclusion, without prior consideration of the results. Each review author independently assessed methodological quality using the Cochrane Incontinence Group's assessment criteria, which include quality of random allocation and concealment, description of drop‐outs and withdrawals, analysis by intention‐to‐treat, and blinding during treatment and at outcome assessment. We resolved any differences of opinion by discussion with a third party.

Data extraction and management

Two review authors independently extracted data from the included trials and cross‐checked the data. We sought clarification from the trialists for data that may have been collected but not reported. We subgrouped trial data by type of incontinence ‐ either urodynamic stress incontinence (USI) based on a urodynamic diagnosis, or stress urinary incontinence (SUI) based upon a symptom classification. Mixed urinary incontinence (MUI) was defined when either type of stress incontinence co‐existed with detrusor overactivity, urge urinary incontinence or other urinary symptoms. We used the International Continence Society terminology (Abrams 2002). In the event, however, all the included trials were limited to women with urodynamic stress incontinence.

Data synthesis

We processed the included trial data as described in the Cochrane Handbook for Systematic Reviews of Interventions (Higgins 2011). When appropriate, we undertook meta‐analysis. We expressed outcomes as negative (i.e. failed rather than cured). For categorical outcomes we related the numbers reporting an outcome to the numbers at risk in each group to derive a risk ratio (RR). For continuous variables we used means and standard deviations to derive a mean difference (MD). We used a fixed‐effect model to calculate pooled estimates and their 95% confidence intervals. We only combined trials if the interventions were similar enough based on clinical criteria. When we suspected important heterogeneity from visual inspection of the results, we used the Chi² test for heterogeneity (at 10%) or the I² statistic (Higgins 2003). If concern about heterogeneity persisted, we planned to use a random‐effects model.

Subgroup analyses included different diagnostic groups (i.e. USI, SUI or MUI), types of operations and groups with and without previous incontinence surgery. We would have carried out sensitivity analysis for individual methodological criteria if the data allowed (e.g. quality of concealment of randomisation), but the data were insufficient. For the purpose of the analysis, we considered the Burch colposuspension and Marshall‐Marchetti‐Krantz operations together.

Results

Description of studies

We updated the first version of this review for Issue 2, 2004. We excluded a further four studies and included one new trial (Palma 1985). In a subsequent update (Issue 2, 2006), we included another trial (Di Palumbo 2003). We have identified no further trials since then.

Thus, we have now identified 10 randomised or quasi‐randomised trials of surgery for urinary incontinence, which included needle suspension in one arm. They were conducted in six countries (UK, USA, Brazil, Greece, Italy and Croatia) and included a total of 864 women, of whom 375 had a needle suspension. Sample sizes ranged from nine to 289. We excluded a total of 11 studies because they were not randomised controlled trials, the women were not all incontinent or the surgical arms included other types of operations (Bump 1995; Bump 1996; Colombo 1997; Corcos 2001; Ishenko 1999; Koonings 1988; Morley 1995; Ramon 1991; Salinas 1994; Vordermark 1979). We excluded one more study because no information was available from the authors to allow a decision to be made about eligibility (Morley 1995), and another because it was a trial of prolapse treatment rather than needle suspension (Goldberg 2001). Details are given in the table of Characteristics of excluded studies.

Nine trials included only women with urodynamic stress incontinence (USI). In one trial women had mixed incontinence (Di Palumbo 2003); three specifically included women with prolapse (Athanassopoulos 1996; Bergman 1989b; Di Palumbo 2003), and only four were restricted to women who had not had previous incontinence surgery (Bergman 1989a; Bergman 1989b; Gilja 1998; Stein 1991). The other six included a mixed population of women, some of whom had previous failed continence surgery. All trials included pre‐ and post‐menopausal women. Long‐term follow‐up was reported in two trials (Bergman 1989a; Di Palumbo 2003).

Types of needle operations

Six different types or modifications of needle suspension were described in the trials:

We classed the Gilja operation as a needle suspension rather than an open retropubic colposuspension for this review. In one trial using three different operations, it was the suture used rather than the operation that was randomised: the authors stated that the type of operation did not affect randomisation or outcomes (Stein 1991). The open abdominal retropubic suspensions were all described as 'Burch colposuspension' except in one trial (German 1992), in which a vagina/obturator shelf repair was used and another where the comparison was with Marshall‐Marchetti‐Krantz (Palma 1985): we classed both as open abdominal retropubic suspensions for this review.

Further details of the trials are reported in the table of Characteristics of included studies.

Risk of bias in included studies

One study used a secure method of concealment of randomisation (sealed envelopes, Di Palumbo 2003), and three studies used a quasi‐randomised method of allocation (birth date (Athanassopoulos 1996); open randomisation list (Gilja 1998); and alternation (Mundy 1983)). The others used 'randomisation lists or tables' without explaining how they were actually used. Women could not be blinded when abdominal operations were compared with vaginal operations. Blinding of outcome assessors was only reported in one trial (Palma 1985).

Baseline comparability of the groups was not mentioned in two studies (Athanassopoulos 1996; Mundy 1983). The others reported that the groups were 'comparable' in terms of age, parity and menopausal status, but four failed to provide specific data (Bergman 1989a; Bergman 1989b; Di Palumbo 2003; Gilja 1998). Only three studies reported drop‐outs: 20 women could not be traced at five years in one trial (Bergman 1989a); in another trial, 58 were lost to follow‐up at three years due to war (Gilja 1998) and four were excluded because they were not followed up in another trial (Stein 1991).

Four studies reported follow‐up of a year or less (Bergman 1989b; Mundy 1983; Stein 1991), one presented data at five years (Bergman 1989a), and some women were followed to six years in another trial (Di Palumbo 2003).

Effects of interventions

1. Needle suspension versus mock procedure

We identified no studies in which needle suspension was compared with a sham or mock procedure, or no alternative intervention.

2. Needle suspension versus conservative interventions

We identified no studies in which needle suspension was compared with a conservative or physical intervention.

3. Needle suspension versus open abdominal retropubic suspension

Needle suspension was compared with open abdominal retropubic suspension in seven trials (Athanassopoulos 1996; Bergman 1989a; Bergman 1989b; German 1992; Gilja 1998; Mundy 1983; Palma 1985). Five compared a needle suspension with a Burch type of colposuspension; one was described as a vagina/obturator shelf repair (German 1992), and the other used a Marshall‐Marchetti Krantz (Palma 1985). Two methods of needle suspension were combined for comparison with colposuspension in one trial (Gilja 1998), although one of them could be regarded as a hybrid of a needle suspension and a colposuspension (termed as 'transvaginal Burch (Gilja) operation' by the authors).

Needle suspension was less effective than colposuspension, based on subjective outcome within one year of surgery (risk ratio (RR) for failure 1.70, 95% confidence interval (CI) 1.11 to 2.60, Analysis 1.1); and after the first year (91/313 (29%) failed after needle suspension versus 47/297 (16%) after open abdominal retropubic suspension; RR 2.00, 95% CI 1.47 to 2.72, Analysis 1.2) (Athanassopoulos 1996; Bergman 1989a; Bergman 1989b; German 1992; Gilja 1998; Mundy 1983; Palma 1985).

Overall, there was no statistically significant difference in peri‐operative complications (haematoma, abscess, infection, pain, urinary tract infection, stitch removal for pain and Dacron sheath removal for infection) after needle procedures (17/75 (23%) versus 12/77 (16%); RR 1.44, 95% CI 0.73 to 2.83, Analysis 1.9), which were reported in three trials (Athanassopoulos 1996; German 1992; Mundy 1983). However, there was significant heterogeneity for this outcome (P value = 0.02, I² = 75%), which may have been due to an unusually low rate of complications after colposuspension in one trial (Mundy 1983).

There were no clear differences between the procedures for any of the other outcome measures, but the confidence intervals around these estimates were wide.

See Analysis 1.1 to Analysis 1.10.

Effect of previous incontinence surgery

Three of the trials included only women who had primary incontinence (i.e. they had not had previous surgery for incontinence) (Bergman 1989a; Bergman 1989b; Gilja 1998). In these trials, women who had an open operation did better after at least one year (57/218 (26%) failed after needle suspension versus 23/190 (12%) after open abdominal retropubic suspension; RR 2.37, 95% CI 1.54 to 3.66, Analysis 2.2). However, none of these trials reported peri‐operative morbidity rates.

Results from the four smaller trials, which included some women who had had previous incontinence surgery, showed the same trend (34/95 (36%) failed after needle suspension versus 24/107 (22%) after open abdominal retropubic suspension; RR 1.61, 95% CI 1.04 to 2.49, Analysis 3.2).

The peri‐operative morbidity data were the same as when all trials were considered together (17/75 (23%) versus 12/77 (16%); RR 1.44, 95% CI 0.73 to 2.83, Analysis 3.8) (Athanassopoulos 1996; German 1992; Mundy 1983; Palma 1985).

4. Needle suspension versus suburethral sling operations

One trial compared Stamey needle suspension with porcine dermis sling (Hilton 1989). This was a small trial with only 10 women in each arm. The women were unsuitable for open abdominal retropubic suspension (the author's preferred procedure) because they had vaginal narrowing secondary to either previous interventions or atrophic vaginitis. Although the trial was too small to address differences in cure rates, sling operations were associated with higher complication rates (9/10 versus 2/10) (Analysis 4.6). These included pyrexia, blood loss, wound infection and pulmonary embolus, need for a permanent suprapubic catheter and more adjuvant therapy, and resulted in a longer stay in hospital (Analysis 4.7).

5. Needle suspension versus anterior vaginal repair

Needle suspension was compared with anterior repair in three trials (Bergman 1989a; Bergman 1989b; Di Palumbo 2003). The performance of the two operations appeared similar in terms of subjective cure rates after 12 months (50/156 versus 64/181; RR 0.86, 95% CI 0.64 to 1.16, Analysis 5.2) and voiding dysfunction, whether the women had prolapse in addition to stress incontinence (Bergman 1989b; Di Palumbo 2003), or not (Bergman 1989a). The numbers were not large, however, and only one objective clinical outcome was reported (no women had long‐term problems with voiding dysfunction after any of the operations, Analysis 5.4).

6. Needle suspension versus laparoscopic colposuspension

We identified no eligible studies in which needle suspension was compared with laparoscopic colposuspension.

7. Needle suspension versus peri‐urethral injections

We identified no eligible studies in which needle suspension was compared with peri‐urethral injections.

8. Needle suspension versus drug treatment (e.g. adrenergic agonists)

We identified no eligible studies in which needle suspension was compared with a drug.

9. One type of needle suspension versus another

One trial involved a comparison between a standard Raz needle suspension and a modified operation involving direct attachment of the sutures to the ileopectineal ligament (termed 'transvaginal Burch (Gilja) operation' by the authors) (Gilja 1998). However, while there were no significant differences in outcomes, the confidence intervals were wide, reflecting the small number of women in the trial (See Analysis 6.1 to Analysis 6.3).

10. Different types of sutures

In one small trial postoperative pain was significantly less at three months in women whose needle suspension was carried out using polytetrafluoroethylene sutures (Goretex) compared with polypropylene (difference in pain score ‐0.92, 95% CI ‐1.77 to ‐0.07, Analysis 7.4) (Stein 1991). The numbers were too small to provide useful information about effectiveness.

Economic outcomes

Although no formal economic outcome measures were reported, some trials reported length of stay (Athanassopoulos 1996; Hilton 1989; Palma 1985), duration to return to normal function (German 1992), or operating time (Palma 1985). However, with the exception of the Hilton trial (where women stayed longer after sling operations, Hilton 1989), we could make no formal statistical comparisons or draw any conclusions.

Discussion

This review is one of a series of reviews of surgical operations for urinary incontinence and it should be viewed in that context (Dean 2006; Glazener 2001; Kirchin 2012; Lapitan 2012; Rehman 2011). Amongst the trials that addressed the effects of needle suspension procedures for stress incontinence, the quality of the trials was poor (three of nine used quasi‐randomised methods and all but one of the remainder did not provide details of the process of randomisation) and the numbers of women who participated were low. Long‐term follow‐up (five years) was only available in two trials (Bergman 1989a; Di Palumbo 2003). Five of the trials included some women who had previous surgery for incontinence, and three included women with prolapse; however, data were not reported separately according to these subgroups.

Outcome measures were generally subjective and limited, with little evidence of reliability and validity. Only one of the trials reported that assessment of outcome was carried out by blinded observers. Patient satisfaction with, and acceptability of, the treatment were not addressed but are important factors in choice of management. No quality of life, mental health or formal economic outcomes were reported (Black 1997; Kelleher 1997), but are recommended for future research. All trials included women with urodynamic stress incontinence only, therefore the effect in women with co‐existing detrusor overactivity or urge incontinence (mixed incontinence) could not be assessed.

Needle suspension versus open abdominal retropubic suspension

Needle suspensions were less successful than open abdominal retropubic suspensions in terms of higher failure rates, although there were no significant differences in other outcome measures. This effect was seen in women with both primary and secondary (after failed primary continence surgery) incontinence.

Needle suspension versus suburethral sling operations

The one small trial that compared needle operations with slings included an atypical population who were unsuitable for more radical surgery (Hilton 1989). There were too few women to provide reliable data about cure rates. Although the sling operations were associated with more postoperative morbidity, the results cannot be generalised to the whole population having surgery because of the atypical nature of the women involved in the trial.

Needle suspension versus anterior vaginal repair

Needle suspension appeared to provide similar cure rates to anterior vaginal repair in women with (Bergman 1989b) and without prolapse (Bergman 1989a), both in the short term and long term, but the numbers were small and clinically important differences could not be ruled out. However, the effects were of the order expected from a review of anterior repair (132/322 (41%) failed after the first year) (Glazener 2001). In the current review, 50/129 (39%) failed after anterior repair versus 46/128 (36%) after needle suspension. This suggests that needle suspension is as effective as anterior repair (but both are less effective than open abdominal retropubic suspension).

One type of needle suspension versus another

In one trial, using direct vision to attach the needle sutures did not significantly improve outcomes, but the numbers were too small to be reliable (Gilja 1998).

Types of sutures

Polytetrafluoroethylene sutures (Goretex) seemed to result in less postoperative pain in the medium term than polypropylene sutures, but the single study was too small to assess continence (Stein 1991).

Outcomes

The primary outcome of effectiveness used in this review was subjective report of failure to cure incontinence. Objective urodynamic outcome measures, for example change in functional urethral length or maximal urethral pressure (Bump 1988; Hilton 1983) were reported in four of the trials (Athanassopoulos 1996; Bergman 1989a; Bergman 1989b; Hilton 1989). These are measurable continuous variables, which allow trials with smaller numbers of participants to obtain relatively precise statistical estimates of any differences. However, they are of limited help in determining optimal treatment because they have no proven correlation with clinical outcome (Meyer 1994; Swift 1995). Until accepted normal values, which correlate with clinical signs and symptoms, are available for these tests, they will not be included in this review.

Morbidity outcomes relevant to surgical complications (such as pain, voiding dysfunction, detrusor overactivity, entero‐rectocoele, wound and urinary infections, length of stay and time to return to normal function) were not consistently reported. Such morbidity is of particular importance in decision‐making when treating benign disease. Data describing treatment failure in terms of need for alternative interventions, or for repeat surgery for incontinence and prolapse, would be particularly useful.

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 1 Number not cured (worse, unchanged or improved) within first year.
Figures and Tables -
Analysis 1.1

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 1 Number not cured (worse, unchanged or improved) within first year.

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 2 Number not cured (worse, unchanged or improved) after first year.
Figures and Tables -
Analysis 1.2

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 2 Number not cured (worse, unchanged or improved) after first year.

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 3 Number not improved (worse or unchanged) within first year.
Figures and Tables -
Analysis 1.3

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 3 Number not improved (worse or unchanged) within first year.

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 4 Number not improved (worse or unchanged) after first year.
Figures and Tables -
Analysis 1.4

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 4 Number not improved (worse or unchanged) after first year.

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 5 Urge symptoms or urge incontinence.
Figures and Tables -
Analysis 1.5

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 5 Urge symptoms or urge incontinence.

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 6 Voiding dysfunction after 3 months.
Figures and Tables -
Analysis 1.6

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 6 Voiding dysfunction after 3 months.

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 7 Detrusor overactivity (objective diagnosis by urodynamics).
Figures and Tables -
Analysis 1.7

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 7 Detrusor overactivity (objective diagnosis by urodynamics).

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 8 New or persistent prolapse.
Figures and Tables -
Analysis 1.8

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 8 New or persistent prolapse.

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 9 Peri‐operative surgical complications.
Figures and Tables -
Analysis 1.9

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 9 Peri‐operative surgical complications.

Study

Needle suspension

Abdominal suspension

Athanassopoulos 1996

Mean length of stay: 3 days (range 6 to 12)

Mean length of stay: 5.8 days (range 4 to 11)

German 1992

Mean length of stay: 7 days
Time to return to normal activity: 7 weeks

Mean length of stay: 8.3 days
Time to return to normal activity: 10.4 weeks

Figures and Tables -
Analysis 1.10

Comparison 1 Needle suspension versus open abdominal retropubic suspension, Outcome 10 Length of stay/time to return to normal function.

Comparison 2 Needle suspension versus open abdominal retropubic suspension (no previous surgery), Outcome 1 Number not cured (worse, unchanged or improved) within first year.
Figures and Tables -
Analysis 2.1

Comparison 2 Needle suspension versus open abdominal retropubic suspension (no previous surgery), Outcome 1 Number not cured (worse, unchanged or improved) within first year.

Comparison 2 Needle suspension versus open abdominal retropubic suspension (no previous surgery), Outcome 2 Number not cured (worse, unchanged or improved) after first year.
Figures and Tables -
Analysis 2.2

Comparison 2 Needle suspension versus open abdominal retropubic suspension (no previous surgery), Outcome 2 Number not cured (worse, unchanged or improved) after first year.

Comparison 2 Needle suspension versus open abdominal retropubic suspension (no previous surgery), Outcome 3 Urge symptoms or urge incontinence.
Figures and Tables -
Analysis 2.3

Comparison 2 Needle suspension versus open abdominal retropubic suspension (no previous surgery), Outcome 3 Urge symptoms or urge incontinence.

Comparison 2 Needle suspension versus open abdominal retropubic suspension (no previous surgery), Outcome 4 New or persistent prolapse.
Figures and Tables -
Analysis 2.4

Comparison 2 Needle suspension versus open abdominal retropubic suspension (no previous surgery), Outcome 4 New or persistent prolapse.

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 1 Number not cured (worse, unchanged or improved) within first year.
Figures and Tables -
Analysis 3.1

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 1 Number not cured (worse, unchanged or improved) within first year.

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 2 Number not cured (worse, unchanged or improved) after first year.
Figures and Tables -
Analysis 3.2

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 2 Number not cured (worse, unchanged or improved) after first year.

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 3 Number not improved (worse or unchanged) within first year.
Figures and Tables -
Analysis 3.3

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 3 Number not improved (worse or unchanged) within first year.

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 4 Number not improved (worse or unchanged) after first year.
Figures and Tables -
Analysis 3.4

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 4 Number not improved (worse or unchanged) after first year.

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 5 Urge symptoms or urge incontinence.
Figures and Tables -
Analysis 3.5

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 5 Urge symptoms or urge incontinence.

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 6 Voiding dysfunction after 3 months.
Figures and Tables -
Analysis 3.6

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 6 Voiding dysfunction after 3 months.

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 7 Detrusor overactivity (objective diagnosis by urodynamics).
Figures and Tables -
Analysis 3.7

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 7 Detrusor overactivity (objective diagnosis by urodynamics).

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 8 Peri‐operative surgical complications.
Figures and Tables -
Analysis 3.8

Comparison 3 Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery), Outcome 8 Peri‐operative surgical complications.

Comparison 4 Needle suspension versus suburethral sling operations, Outcome 1 Number not cured (worse, unchanged or improved) within first year.
Figures and Tables -
Analysis 4.1

Comparison 4 Needle suspension versus suburethral sling operations, Outcome 1 Number not cured (worse, unchanged or improved) within first year.

Comparison 4 Needle suspension versus suburethral sling operations, Outcome 2 Number not cured (worse, unchanged or improved) after first year.
Figures and Tables -
Analysis 4.2

Comparison 4 Needle suspension versus suburethral sling operations, Outcome 2 Number not cured (worse, unchanged or improved) after first year.

Comparison 4 Needle suspension versus suburethral sling operations, Outcome 3 Urge symptoms or urge incontinence.
Figures and Tables -
Analysis 4.3

Comparison 4 Needle suspension versus suburethral sling operations, Outcome 3 Urge symptoms or urge incontinence.

Comparison 4 Needle suspension versus suburethral sling operations, Outcome 4 Voiding dysfunction after 3 months.
Figures and Tables -
Analysis 4.4

Comparison 4 Needle suspension versus suburethral sling operations, Outcome 4 Voiding dysfunction after 3 months.

Comparison 4 Needle suspension versus suburethral sling operations, Outcome 5 Detrusor overactivity (objective diagnosis by urodynamics).
Figures and Tables -
Analysis 4.5

Comparison 4 Needle suspension versus suburethral sling operations, Outcome 5 Detrusor overactivity (objective diagnosis by urodynamics).

Comparison 4 Needle suspension versus suburethral sling operations, Outcome 6 Peri‐operative surgical complications.
Figures and Tables -
Analysis 4.6

Comparison 4 Needle suspension versus suburethral sling operations, Outcome 6 Peri‐operative surgical complications.

Comparison 4 Needle suspension versus suburethral sling operations, Outcome 7 Length of inpatient stay.
Figures and Tables -
Analysis 4.7

Comparison 4 Needle suspension versus suburethral sling operations, Outcome 7 Length of inpatient stay.

Comparison 5 Needle suspension versus anterior vaginal repair, Outcome 1 Number not cured (worse, unchanged or improved) within first year.
Figures and Tables -
Analysis 5.1

Comparison 5 Needle suspension versus anterior vaginal repair, Outcome 1 Number not cured (worse, unchanged or improved) within first year.

Comparison 5 Needle suspension versus anterior vaginal repair, Outcome 2 Number not cured (worse, unchanged or improved) after first year.
Figures and Tables -
Analysis 5.2

Comparison 5 Needle suspension versus anterior vaginal repair, Outcome 2 Number not cured (worse, unchanged or improved) after first year.

Comparison 5 Needle suspension versus anterior vaginal repair, Outcome 3 Urge symptoms or urge incontinence.
Figures and Tables -
Analysis 5.3

Comparison 5 Needle suspension versus anterior vaginal repair, Outcome 3 Urge symptoms or urge incontinence.

Comparison 5 Needle suspension versus anterior vaginal repair, Outcome 4 Voiding dysfunction after 3 months.
Figures and Tables -
Analysis 5.4

Comparison 5 Needle suspension versus anterior vaginal repair, Outcome 4 Voiding dysfunction after 3 months.

Comparison 5 Needle suspension versus anterior vaginal repair, Outcome 5 Peri‐operative surgical complications.
Figures and Tables -
Analysis 5.5

Comparison 5 Needle suspension versus anterior vaginal repair, Outcome 5 Peri‐operative surgical complications.

Comparison 5 Needle suspension versus anterior vaginal repair, Outcome 6 New or persistent prolapse.
Figures and Tables -
Analysis 5.6

Comparison 5 Needle suspension versus anterior vaginal repair, Outcome 6 New or persistent prolapse.

Comparison 6 One type of needle suspension versus another type of needle suspension, Outcome 1 Number not cured (worse, unchanged or improved) within first year.
Figures and Tables -
Analysis 6.1

Comparison 6 One type of needle suspension versus another type of needle suspension, Outcome 1 Number not cured (worse, unchanged or improved) within first year.

Comparison 6 One type of needle suspension versus another type of needle suspension, Outcome 2 Number not cured (worse, unchanged or improved) after first year.
Figures and Tables -
Analysis 6.2

Comparison 6 One type of needle suspension versus another type of needle suspension, Outcome 2 Number not cured (worse, unchanged or improved) after first year.

Comparison 6 One type of needle suspension versus another type of needle suspension, Outcome 3 Urge symptoms or urge incontinence.
Figures and Tables -
Analysis 6.3

Comparison 6 One type of needle suspension versus another type of needle suspension, Outcome 3 Urge symptoms or urge incontinence.

Comparison 7 One type of suture versus another type of suture, Outcome 1 Number not cured (worse, unchanged or improved) within first year.
Figures and Tables -
Analysis 7.1

Comparison 7 One type of suture versus another type of suture, Outcome 1 Number not cured (worse, unchanged or improved) within first year.

Comparison 7 One type of suture versus another type of suture, Outcome 2 Number not improved (worse or unchanged) within first year.
Figures and Tables -
Analysis 7.2

Comparison 7 One type of suture versus another type of suture, Outcome 2 Number not improved (worse or unchanged) within first year.

Comparison 7 One type of suture versus another type of suture, Outcome 3 Urge symptoms or urge incontinence.
Figures and Tables -
Analysis 7.3

Comparison 7 One type of suture versus another type of suture, Outcome 3 Urge symptoms or urge incontinence.

Comparison 7 One type of suture versus another type of suture, Outcome 4 Pain score.
Figures and Tables -
Analysis 7.4

Comparison 7 One type of suture versus another type of suture, Outcome 4 Pain score.

Comparison 1. Needle suspension versus open abdominal retropubic suspension

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Number not cured (worse, unchanged or improved) within first year Show forest plot

5

517

Risk Ratio (M‐H, Fixed, 95% CI)

1.70 [1.11, 2.60]

1.1 Objective/genuine stress incontinence (only)

5

517

Risk Ratio (M‐H, Fixed, 95% CI)

1.70 [1.11, 2.60]

1.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2 Number not cured (worse, unchanged or improved) after first year Show forest plot

7

610

Risk Ratio (M‐H, Fixed, 95% CI)

2.00 [1.47, 2.72]

2.1 Objective/genuine stress incontinence (only)

7

610

Risk Ratio (M‐H, Fixed, 95% CI)

2.00 [1.47, 2.72]

2.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3 Number not improved (worse or unchanged) within first year Show forest plot

1

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.75 [0.07, 7.73]

3.1 Objective/genuine stress incontinence (only)

1

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.75 [0.07, 7.73]

3.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4 Number not improved (worse or unchanged) after first year Show forest plot

1

51

Risk Ratio (M‐H, Fixed, 95% CI)

1.5 [0.37, 6.04]

4.1 Objective/genuine stress incontinence (only)

1

51

Risk Ratio (M‐H, Fixed, 95% CI)

1.5 [0.37, 6.04]

4.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5 Urge symptoms or urge incontinence Show forest plot

4

297

Risk Ratio (M‐H, Fixed, 95% CI)

1.80 [0.71, 4.56]

5.1 Objective/genuine stress incontinence (only)

4

297

Risk Ratio (M‐H, Fixed, 95% CI)

1.80 [0.71, 4.56]

5.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6 Voiding dysfunction after 3 months Show forest plot

4

202

Risk Ratio (M‐H, Fixed, 95% CI)

2.12 [0.81, 5.55]

6.1 Objective/genuine stress incontinence (only)

4

202

Risk Ratio (M‐H, Fixed, 95% CI)

2.12 [0.81, 5.55]

6.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

7 Detrusor overactivity (objective diagnosis by urodynamics) Show forest plot

2

101

Risk Ratio (M‐H, Fixed, 95% CI)

2.91 [0.73, 11.58]

7.1 Objective/genuine stress incontinence (only)

2

101

Risk Ratio (M‐H, Fixed, 95% CI)

2.91 [0.73, 11.58]

7.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

7.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

8 New or persistent prolapse Show forest plot

1

72

Risk Ratio (M‐H, Fixed, 95% CI)

2.24 [0.21, 23.57]

8.1 Objective/genuine stress incontinence (only)

1

72

Risk Ratio (M‐H, Fixed, 95% CI)

2.24 [0.21, 23.57]

8.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

8.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

9 Peri‐operative surgical complications Show forest plot

3

152

Risk Ratio (M‐H, Fixed, 95% CI)

1.44 [0.73, 2.83]

9.1 Objective/genuine stress incontinence (only)

3

152

Risk Ratio (M‐H, Fixed, 95% CI)

1.44 [0.73, 2.83]

9.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

9.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

10 Length of stay/time to return to normal function Show forest plot

Other data

No numeric data

Figures and Tables -
Comparison 1. Needle suspension versus open abdominal retropubic suspension
Comparison 2. Needle suspension versus open abdominal retropubic suspension (no previous surgery)

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Number not cured (worse, unchanged or improved) within first year Show forest plot

3

417

Risk Ratio (M‐H, Fixed, 95% CI)

2.05 [1.20, 3.50]

1.1 Objective/genuine stress incontinence (only)

3

417

Risk Ratio (M‐H, Fixed, 95% CI)

2.05 [1.20, 3.50]

1.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2 Number not cured (worse, unchanged or improved) after first year Show forest plot

3

408

Risk Ratio (M‐H, Fixed, 95% CI)

2.37 [1.54, 3.66]

2.1 Objective/genuine stress incontinence (only)

3

408

Risk Ratio (M‐H, Fixed, 95% CI)

2.37 [1.54, 3.66]

2.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3 Urge symptoms or urge incontinence Show forest plot

1

146

Risk Ratio (M‐H, Fixed, 95% CI)

2.49 [0.55, 11.30]

3.1 Objective/genuine stress incontinence (only)

1

146

Risk Ratio (M‐H, Fixed, 95% CI)

2.49 [0.55, 11.30]

3.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4 New or persistent prolapse Show forest plot

1

72

Risk Ratio (M‐H, Fixed, 95% CI)

2.24 [0.21, 23.57]

4.1 Objective/genuine stress incontinence (only)

1

72

Risk Ratio (M‐H, Fixed, 95% CI)

2.24 [0.21, 23.57]

4.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

Figures and Tables -
Comparison 2. Needle suspension versus open abdominal retropubic suspension (no previous surgery)
Comparison 3. Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery)

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Number not cured (worse, unchanged or improved) within first year Show forest plot

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

1.12 [0.55, 2.29]

1.1 Objective/genuine stress incontinence (only)

2

100

Risk Ratio (M‐H, Fixed, 95% CI)

1.12 [0.55, 2.29]

1.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2 Number not cured (worse, unchanged or improved) after first year Show forest plot

4

202

Risk Ratio (M‐H, Fixed, 95% CI)

1.61 [1.04, 2.49]

2.1 Objective/genuine stress incontinence (only)

4

202

Risk Ratio (M‐H, Fixed, 95% CI)

1.61 [1.04, 2.49]

2.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3 Number not improved (worse or unchanged) within first year Show forest plot

1

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.75 [0.07, 7.73]

3.1 Objective/genuine stress incontinence (only)

1

50

Risk Ratio (M‐H, Fixed, 95% CI)

0.75 [0.07, 7.73]

3.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4 Number not improved (worse or unchanged) after first year Show forest plot

1

51

Risk Ratio (M‐H, Fixed, 95% CI)

1.5 [0.37, 6.04]

4.1 Objective/genuine stress incontinence (only)

1

51

Risk Ratio (M‐H, Fixed, 95% CI)

1.5 [0.37, 6.04]

4.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5 Urge symptoms or urge incontinence Show forest plot

3

151

Risk Ratio (M‐H, Fixed, 95% CI)

1.40 [0.42, 4.59]

5.1 Objective/genuine stress incontinence (only)

3

151

Risk Ratio (M‐H, Fixed, 95% CI)

1.40 [0.42, 4.59]

5.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6 Voiding dysfunction after 3 months Show forest plot

4

202

Risk Ratio (M‐H, Fixed, 95% CI)

2.12 [0.81, 5.55]

6.1 Objective/genuine stress incontinence (only)

4

202

Risk Ratio (M‐H, Fixed, 95% CI)

2.12 [0.81, 5.55]

6.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

7 Detrusor overactivity (objective diagnosis by urodynamics) Show forest plot

2

101

Risk Ratio (M‐H, Fixed, 95% CI)

2.91 [0.73, 11.58]

7.1 Objective/genuine stress incontinence (only)

2

101

Risk Ratio (M‐H, Fixed, 95% CI)

2.91 [0.73, 11.58]

7.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

7.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

8 Peri‐operative surgical complications Show forest plot

3

152

Risk Ratio (M‐H, Fixed, 95% CI)

1.44 [0.73, 2.83]

8.1 Objective/genuine stress incontinence (only)

3

152

Risk Ratio (M‐H, Fixed, 95% CI)

1.44 [0.73, 2.83]

8.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

8.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

Figures and Tables -
Comparison 3. Needle suspension versus open abdominal retropubic suspension (mixed population, some after previous surgery)
Comparison 4. Needle suspension versus suburethral sling operations

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Number not cured (worse, unchanged or improved) within first year Show forest plot

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

2.0 [0.21, 18.69]

1.1 Objective/genuine stress incontinence (only)

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

2.0 [0.21, 18.69]

1.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2 Number not cured (worse, unchanged or improved) after first year Show forest plot

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

3.0 [0.37, 24.17]

2.1 Objective/genuine stress incontinence (only)

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

3.0 [0.37, 24.17]

2.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3 Urge symptoms or urge incontinence Show forest plot

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

0.6 [0.19, 1.86]

3.1 Objective/genuine stress incontinence (only)

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

0.6 [0.19, 1.86]

3.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4 Voiding dysfunction after 3 months Show forest plot

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

0.5 [0.12, 2.14]

4.1 Objective/genuine stress incontinence (only)

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

0.5 [0.12, 2.14]

4.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5 Detrusor overactivity (objective diagnosis by urodynamics) Show forest plot

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

0.5 [0.05, 4.67]

5.1 Objective/genuine stress incontinence (only)

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

0.5 [0.05, 4.67]

5.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6 Peri‐operative surgical complications Show forest plot

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

0.22 [0.06, 0.78]

6.1 Objective/genuine stress incontinence (only)

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

0.22 [0.06, 0.78]

6.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

7 Length of inpatient stay Show forest plot

1

20

Mean Difference (IV, Fixed, 95% CI)

‐13.0 [‐19.00, ‐5.00]

7.1 Objective/genuine stress incontinence (only)

1

20

Mean Difference (IV, Fixed, 95% CI)

‐13.0 [‐19.00, ‐5.00]

7.2 Subjective stress incontinence (only)

0

0

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

7.3 Mixed incontinence

0

0

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

Figures and Tables -
Comparison 4. Needle suspension versus suburethral sling operations
Comparison 5. Needle suspension versus anterior vaginal repair

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Number not cured (worse, unchanged or improved) within first year Show forest plot

2

266

Risk Ratio (M‐H, Fixed, 95% CI)

0.96 [0.63, 1.46]

1.1 Objective/genuine stress incontinence (only)

2

266

Risk Ratio (M‐H, Fixed, 95% CI)

0.96 [0.63, 1.46]

1.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.3 Mixed incontinence

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2 Number not cured (worse, unchanged or improved) after first year Show forest plot

3

337

Risk Ratio (M‐H, Fixed, 95% CI)

0.86 [0.64, 1.16]

2.1 Objective/genuine stress incontinence (only)

2

257

Risk Ratio (M‐H, Fixed, 95% CI)

0.93 [0.68, 1.26]

2.2 Subjective stress incontinence (only)

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2.3 Mixed incontinence

1

80

Risk Ratio (M‐H, Fixed, 95% CI)

0.53 [0.19, 1.46]

3 Urge symptoms or urge incontinence Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

3.1 Objective/genuine stress incontinence (only)

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.2 Subjective stress incontinence (only)

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.3 Mixed incontinence

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4 Voiding dysfunction after 3 months Show forest plot

3

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

4.1 Objective/genuine stress incontinence (only)

2

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.2 Subjective stress incontinence (only)

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.3 Mixed incontinence

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5 Peri‐operative surgical complications Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

5.1 Objective/genuine stress incontinence (only)

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.2 Subjective stress incontinence (only)

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.3 Mixed incontinence

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6 New or persistent prolapse Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

6.1 Objective/genuine stress incontinence (only)

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6.2 Subjective stress incontinence (only)

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6.3 Mixed incontinence

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

Figures and Tables -
Comparison 5. Needle suspension versus anterior vaginal repair
Comparison 6. One type of needle suspension versus another type of needle suspension

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Number not cured (worse, unchanged or improved) within first year Show forest plot

1

90

Risk Ratio (M‐H, Fixed, 95% CI)

2.87 [0.31, 26.56]

1.1 Raz versus transvaginal Burch (Gilja)

1

90

Risk Ratio (M‐H, Fixed, 95% CI)

2.87 [0.31, 26.56]

2 Number not cured (worse, unchanged or improved) after first year Show forest plot

1

90

Risk Ratio (M‐H, Fixed, 95% CI)

1.67 [0.53, 5.32]

2.1 Raz versus transvaginal Burch (Gilja)

1

90

Risk Ratio (M‐H, Fixed, 95% CI)

1.67 [0.53, 5.32]

3 Urge symptoms or urge incontinence Show forest plot

1

90

Risk Ratio (M‐H, Fixed, 95% CI)

1.59 [0.40, 6.28]

3.1 Raz versus transvaginal Burch (Gilja)

1

90

Risk Ratio (M‐H, Fixed, 95% CI)

1.59 [0.40, 6.28]

Figures and Tables -
Comparison 6. One type of needle suspension versus another type of needle suspension
Comparison 7. One type of suture versus another type of suture

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Number not cured (worse, unchanged or improved) within first year Show forest plot

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

0.17 [0.01, 2.94]

2 Number not improved (worse or unchanged) within first year Show forest plot

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

0.4 [0.02, 8.78]

3 Urge symptoms or urge incontinence Show forest plot

1

20

Risk Ratio (M‐H, Fixed, 95% CI)

0.24 [0.01, 4.44]

4 Pain score Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Subtotals only

4.1 At one month

1

19

Mean Difference (IV, Fixed, 95% CI)

‐0.60 [‐1.87, 0.67]

4.2 At three months

1

20

Mean Difference (IV, Fixed, 95% CI)

‐0.92 [‐1.77, ‐0.07]

Figures and Tables -
Comparison 7. One type of suture versus another type of suture