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Study Title and Description

Risk factors for rejection of suburethral slings for stress urinary incontinence: a case-control study



Key Questions Addressed
2 Sling Adverse Events
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Primary Publication Information
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TitleData
Title Risk factors for rejection of suburethral slings for stress urinary incontinence: a case-control study
Author Persson J, Constin I, Wolner-Hanssen, P.
Country University Hospital of Lund (Sweden), dept of OBGYN
Year 2002
Numbers Pubmed ID: 12039125
1111 (internal)

Secondary Publication Information
There are currently no secondary publications defined for this study.


Extraction Form: Sling Adverse Events
Arms
No arms have been defined in this extraction form.

Design Details
Question... Follow Up Answer Follow-up Answer
Study Type Retrospective Cohort (all received same sling)
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Study Name none noted
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Study Country Sweden
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Sling Category Retropubic synthetic
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Multicenter? No
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Institution Type Academic hospital
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No. of Surgeons Performing the Procedures Unclear/Not reported
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Surgeons' Training Not reported
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Residents or Fellows Performing the Surgery? Unclear/Not reported
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Adverse Event Ascertainment Unclear/Not reported
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Was the Clavien-Dindo Classification of Surgical Complications system used? No / Not reported
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Was a data safety monitoring board used? No / Not reported
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Study Sponsor/Funding Not reported
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Comments (overall study) There is no description of adverse events in this study with the exception of mesh erosion ("sling rejection")
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Results & Comparisons

No Results found.
Adverse Events
Arm or Total Title Description Follow-up time In-hospital or After discharge Is event serious? Reported definition of serious event Number affected Number at risk (analyzed) Difference between 2 slings (eg, OR/RR or %, with 95% CI) Reported P value between slings Comments
Total Mesh erosion/extrusion/exposure/granulation tissue Surgery in 1991-1992 Minimum 24 months, median 38, range 24-98 months After discharge No Not defined 15 35 n/a n/a
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Total Mesh erosion/extrusion/exposure/granulation tissue Surgery in 1993 Minimum 24 months, median 38, range 24-98 monthsMinimum 24 months, median 38, range 24-98 months After discharge No Not defined 18 80 n/a n/a
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Total Mesh erosion/extrusion/exposure/granulation tissue Surgery in 1994 Minimum 24 months, median 38, range 24-98 months After discharge No Not defined 6 85 n/a n/a
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Total Mesh erosion/extrusion/exposure/granulation tissue Surgery in 1995 Minimum 24 months, median 38, range 24-98 months After discharge No Not defined 0 34 n/a n/a
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Total Mesh erosion/extrusion/exposure/granulation tissue Surgery in 1996 Minimum 24 months, median 38, range 24-98 months After discharge No Not defined 2 57 n/a n/a
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Total Mesh erosion/extrusion/exposure/granulation tissue Surgery in 1997 Minimum 24 months, median 38, range 24-98 months After discharge No Not defined 2 47 n/a n/a
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Total Mesh erosion/extrusion/exposure/granulation tissue Surgery in 1998 Minimum 24 months, median 38, range 24-98 months After discharge No Not defined 4 48 n/a n/a
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Total Mesh erosion/extrusion/exposure/granulation tissue Entire study period (1991-1998) Minimum 24 months, median 38, range 24-98 months After discharge No Not defined 47 386 n/a n/a
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Total
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