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ePoster Display

786P - The impact of urine bladder catheterization after radical hysterectomy: Understanding patients’ experience

Date

16 Sep 2021

Session

ePoster Display

Topics

Tumour Site

Cervical Cancer

Presenters

Nicoline Schuur

Citation

Annals of Oncology (2021) 32 (suppl_5): S725-S772. 10.1016/annonc/annonc703

Authors

N. Schuur, M. Vrijhof, C.B. Van de Berg, H.J. Beekhuizen, H.C. van Doorn

Author affiliations

  • Gynacology Oncology, Erasmus MC - Daniel den Hoed Cancer Center, 3075 EA - Rotterdam/NL

Resources

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Abstract 786P

Background

Postoperative bladder dysfunction is a common phenomenon after radical hysterectomy (RAH) in patients with cervical cancer. Post-operatively, women receive a transurethral or suprapubic catheter.

Methods

A questionnaire with 19 items was sent to 62 women who underwent RAH between January 2017 and July 2020 at the Erasmus MC Cancer Institute in Rotterdam, the Netherlands. Questions regarding information received, catheter-related problems, and emotional distress were surveyed using a four-point Likert scale. For analysis, the two lowest and two highest outcomes were combined. Further, women were encouraged to share any comments. The study was approved by the ethical board of the Erasmus MC.

Results

Forty- seven women responded (75%). Insufficient information on catheter use was reported by approximately 20%. A high or very high score was given for frustration by 36%, shame by 21%, fear by 11%, and movement restrictions by 28%. Overall, these were more common in women with a transurethral (n = 29) compared to an suprapubic catheter (n = 18). Additional information in the free text box made it clear that postoperative micturition and catheter- relates problems have a significant impact on quality of life.

Conclusions

Women in this study reported more sorrow and problems related to postoperative catheterization than expected. These results emphasize the need to discuss these issues with our patients, to learn more about their needs, and ultimately to improve the perioperative protocol and thereby reduce the burden on the patients.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

H.C. van Doorn.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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