BMI and specimen weight: impact on personalized risk profiling for optimized informed consent in breast reduction surgery?

Raimund Winter, Frederike Reischies, Alexandru Tuca, Paul Wurzer, Christian Schubert, Christina Wolfsberger, Theresa Margarethe Rienmüller, Herwig Friedl, Michaela Sljivich, Lars-P. Kamolz

Research output: Contribution to journalArticlepeer-review

Abstract

We aimed to evaluate the interaction between individual risk factors and institutional complication rates after reduction mammaplasties to develop a chart for a personalized written patient informed consent.
We retrospectively reviewed charts of 804 patients who underwent bilateral breast reduction between 2005 and 2015. The Clavien-Dindo classification was used to classify postoperative complications. Relevant predictors were found by applying a stepwise variable selection procedure. Multilevel predictors were assessed through chi-square tests on the respective deviance reductions.
486 patients were included. The most common complications were wound healing problems (n=270/56%), foreign body reactions (n=58/12%), wound infections (n=45/9,3%) and fat tissue necrosis (n= 41/8%). The risk factors for the personalized patient chart for the most common complications influencing the preoperative informed consent were: smoking, operative technique, resection weight for wound healing problems; body mass index and allergies for wound infections; and patients’ age, resection weight for fat tissue necrosis.
The resultant chart of institutionally encountered most common complications based on individual risk factors is a graphical template for obtaining patient informed consent in the future. Whether this approach influences patient information retainment, incidence of filed lawsuits or behavioral change needs to be prospectively tested in future studies.
Original languageEnglish
Article number12690
JournalScientific Reports
Volume9
DOIs
Publication statusPublished - Sept 2019

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