The study objective is to improve the current and local standard antiseptic treatment by adjusting the antiseptic agent to the antimicrobial resistance testing result, accordingly. Currently, resistance testing will only be performed for the treatment with antibiotics.
Complications like bacterial wound colonization and infections in wound treatment are still a serious problem. Several therapy approaches are available to treat these complications, e.g. surgical wound debridement, antimicrobial therapy that can be divided into a local and a systemic antisepsis. The local antisepsis (the local utilization of antiseptics directly to the wound) is in many ways advantageous to the systemic antisepsis (orally or intravenously administered antibiotics): e. g. the direct contact of the antiseptic to the bacteria at the site of infection whereas antibiotics may not sufficiently reach the wound due to limited blood perfusion of wounds; growing utilization of systemic antisepsis also leads to an increasing number of resistant bacteria worldwide. To the concerns of many specialists, the first pan-resistant bacterial strain which is resistant to all available antibiotics including colistin was recently published. In future, the role of local antisepsis therefore becomes more important in the antimicrobial treatment. Luckily, resistances of local antiseptics occur slowly due to the chemical and structural characteristics of antiseptics but even resistances of bacteria to antiseptics were reported. Unlike the antimicrobial resistance testing for antibiotics that is done in the clinical routine, such testing is not a standard procedure for antiseptics for no obvious reason. The utilization of antiseptics is determined by the availability of products provided within the institution and preferences of the clinician. Thus, it is unknown whether the chosen antiseptic has any bactericidal effect on the confirmed bacteria. University Hospital RWTH Aachen Wound Care only uses polyhexanide and octenisept. Iodine-containing preparations are explicitly not desired.Improvement (bacteria reduction, acceleration of wound healing) of the local antiseptic therapy by adapting the antiseptic to the results of antimicrobial resistance testing. Antimicrobial resistance testing has so far only been used to adapt systemic antibiotic therapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Swab probes of wounds will be taken upon study inclusion and analysed for resistance on Octenisept and Serasept. If the patient indicates resistance on one of the antiseptics, he/she will receive the other antiseptic for wound dressings
University Hospital RWTH Aachen
Aachen, North Rhine-Westphalia, Germany
Change in bacteria rate
determination of the relative proportion of isolates to the total flora in the wound
Time frame: up to 12 months
Incidence of wound related adverse events
review of medical charts
Time frame: up to 12 months
Change in Pressure Ulcers: Scale for Healing (PUSH) score
score 0-17; 17=big and severe wound
Time frame: up to 12 months
Change in Bates-Jensen Score
Score 13-65; 13-20=minimal severity class; 41-65 extreme severity class
Time frame: up to 12 months
Laboratory Parameters - Change in C-reactive protein (CRP)
mg/L
Time frame: up to 12 months
Laboratory Parameters - Change in Leukocytes
10⁹/L or /nL
Time frame: up to 12 months
Laboratory Parameters - Change in hemoglobin
g/dl
Time frame: up to 12 months
Laboratory Parameters - Change in hematokrit
Time frame: up to 12 months
Laboratory Parameters - Change in creatinine
µmol/L or mg/dl
Time frame: up to 12 months
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Laboratory Parameters - Change in glomerular filtration rate (GFR)
ml/min/1,73m\^2
Time frame: up to 12 months
Laboratory Parameters - Change in Uric acid
mg/dl
Time frame: up to 12 months
Laboratory Parameters - Change in glutamic-pyruvic transaminase (GPT)
IU/L
Time frame: up to 12 months
Laboratory Parameters - Change in Glutamat-Oxalacetat- Transaminase (GOT)
IU/L
Time frame: up to 12 months
Laboratory Parameters - Change in Glucose
mmil/L or mg/dl
Time frame: up to 12 months
Hospital length of stay
from study inclusion until hospital discharge
Time frame: up to 12 months
Rate of antibiotics used
chart review
Time frame: up to 12 months
Length of bed confinement
chart review
Time frame: up to 12 months