Cited by 5Pelvic floor disorders treatmentsGastrointestinal motility and disordersEnhanced Recovery After Surgery

Bowel preparation prior to minimally invasive sacrocolpopexy: a randomized controlled trial

Open access
Sassani, Jessica C., Kantartzis, Kelly, Wu, Liwen, Fabio, Anthony, Zyczynski, Halina M.·2020·International Urogynecology Journal

Abstract

Introduction and hypothesis The objective was to determine if a bowel preparation prior to minimally invasive sacrocolpopexy (MIS) influences post-operative constipation symptoms. We hypothesized that women who underwent a bowel preparation would have an improvement in post-operative defecatory function.Methods In this randomized controlled trial, women undergoing MIS received a pre-operative bowel preparation or no bowel preparation. Our primary outcome was post-operative constipation measured by the Patient Assessment of Constipation Symptoms (PAC-SYM) 2 weeks post-operatively. Secondary outcomes included surgeon's perception of case difficulty. Both intention-to-treat (ITT) and per-protocol analyses (PPA) were performed. Analyses were carried out using t test, Fisher's exact test, the Wilcoxon test and the Chi-squared test.Results Of 105 enrolled women, 95 completed follow-up (43 preparation and 52 no preparation). Baseline characteristics and rates of complications were similar. No differences were noted on ITT. The post-operative abdominal PAC-SYM subscale was closer to baseline for women who received a bowel preparation on PPA (change in score 0.74 vs 1.08, p = 0.045). Women who underwent a preparation were less likely to report strain (6.0% vs 26.7%, p = 0.009) or type 1 Bristol stool on their first post-operative bowel movement (4.3% vs 17.5%, p = 0.047). Surgeons were more likely to rate the complexity of the case as "more difficult than average" (54.4% vs 40.1%, p = 0.027) in those without a bowel preparation.Conclusions Although there was no difference in ITT analysis, women who underwent a bowel preparation prior to MIS demonstrated benefit to post-operative defecatory function with a corresponding improvement in surgeon's perception of case complexity.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1007/s00192-019-04120-7

Cites

15 of 15 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • In women undergoing POP surgery, bowel preparation versus no bowel preparation may result in no clinically relevant difference in readmission to hospital within 30 days (OR 0.16, 95% CI 0.01 to 3.24; 1 study, 95 women).

    “Based on evidence from a single trial (Sassani 2020), there may be no clinically relevant difference in readmission to hospital rates between the two groups (OR 0.16, 95% CI 0.01 to 3.24; 1 study, 95 women; Analysis 5.2).”

    From Perioperative interventions in pelvic organ prolapse surgery (2025) · cites this paper as Sassani 2020

    The Results report 95 women with outcome data and say readmissions were similar between the bowel-preparation and no-preparation groups (p>0.05). Our copy does not report a 30-day readmission window or the cited odds ratio and confidence interval, so those specifics are not supported by this source. (LLM, conf=0.86)

    Experimental — accuracy not yet measured
  • In Sassani 2020, the randomisation method was computer randomisation.

    “Randomisation method: computer randomisation”

    From Perioperative interventions in pelvic organ prolapse surgery (2025) · cites this paper as Sassani 2020

    The Materials and Methods section says participants were assigned by simple randomization in a 1:1 ratio, with research staff randomizing them when surgery was scheduled. It does not say that the randomization was computer-generated; the use of a computer remains unverified. (LLM, conf=0.83)

    Experimental — accuracy not yet measured
  • In Sassani 2020, the risk of attrition bias from incomplete outcome data was high.

    “Incomplete outcome data (attrition bias) All outcomes High risk 51/52 Group A; however, 45/54 (17%) in Group B”

    From Perioperative interventions in pelvic organ prolapse surgery (2025) · cites this paper as Sassani 2020

    The Results (page unavailable) report incomplete outcome data: 95 of 105 participants provided it. They give 43 participants in the prep group and 52 in the no-prep group, not the cited 51/52 and 45/54 figures. The paper does not itself rate attrition bias as high risk. (LLM, conf=0.86)

    Experimental — accuracy not yet measured
  • In Sassani 2020, the risk of performance bias from blinding of participants and personnel was high.

    “Blinding of participants and personnel (performance bias) All outcomes High risk Unable to be blinded”

    From Perioperative interventions in pelvic organ prolapse surgery (2025) · cites this paper as Sassani 2020

    The Discussion (page unavailable) says a placebo would have masked patients to their assignment, supporting concern about participant blinding. But Materials and Methods (page unavailable) explicitly says physicians and fellows were blinded to group assignment. The paper therefore does not support the claim that both participants and personnel were unable to be blinded; it does not itself assign a high-risk performance-bias rating. (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • In Sassani 2020, the risk of detection bias from blinding of outcome assessment was low.

    “Blinding of outcome assessment (detection bias) All outcomes Low risk Blinded”

    From Perioperative interventions in pelvic organ prolapse surgery (2025) · cites this paper as Sassani 2020

    Materials and Methods (page unavailable) says physicians and fellows were blinded to group assignment, supporting blinding for the surgeon-assessed outcomes. But the primary constipation outcome was patient-reported, and the Discussion says a placebo would have masked patients to their assignment. The paper therefore does not support the citing sentence’s blanket assessment of low detection-bias risk for all outcomes. (LLM, conf=0.88)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Sassani, J. C., Kantartzis, K., Wu, L., Fabio, A., & Zyczynski, H. M.
Affiliations
  • University of Pittsburgh (US)
  • University of Arizona (US)
Corresponding author
Sassani, Jessica C.
Venue
International Urogynecology Journal
Published
2019-11-26
Volume
31
Issue
7
Pages
1305-1313
ISSN
  • 0937-3462 (ISSN-L)
  • 1433-3023
OpenAlex
W2990528709
Cited by
5
References
15
Citations by year
2025: 1 · 2024: 1 · 2023: 1 · 2022: 1 · 2020: 1
FWCI
0.38
Type
journal article
Language
en
Open access
Locations
  • International Urogynecology Journal (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Institutes of Health (UL1TR001857)
Topics
  • Health Sciences › Medicine › Rheumatology › Pelvic floor disorders treatments
  • Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
  • Health Sciences › Medicine › Surgery › Enhanced Recovery After Surgery
Keywords
bowel preparation, postoperative constipation, pelvic organ prolapse surgery, straining during defecation, Bristol stool scale, preoperative bowel preparation
MeSH terms
Constipation, Female, Humans, Postoperative Period, Treatment Outcome

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review